A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3686e59



Internal ID22764906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157547652..157547729hg38UCSC Ensembl
chr6:157968684..157968761hg19UCSC Ensembl
chr6:157888672..157888749hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3878
hg1978
hg1878
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3395081, esv3425815
SamplesNA18502, NA12717, NA18947, NA11995, NA18861, NA18592, NA18508, NA10851, NA12414, NA18561, NA18507, NA11931, NA12045, NA18486, NA12751, NA18545, NA19190, NA18870, NA18526, NA12750, NA12155, NA07346, NA19005, NA18944, NA18940, NA18550, NA18519, NA12891, NA18558, NA18547, NA11918, NA07347, NA19138, NA18949, NA12761, NA12156, NA19238, NA11994, NA18520, NA19239, NA11993, NA10847, NA12878, NA18516, NA18579, NA18871, NA18572, NA18907, NA18537, NA19114, NA11919, NA18499, NA18856, NA18912, NA12892, NA18853, NA19099, NA19257, NA19225, NA12144, NA18523, NA18593, NA12043, NA18608, NA18542, NA18909, NA11881, NA19108, NA18961, NA19147, NA18517, NA19240, NA07051, NA18943, NA07037, NA18501, NA19093, NA19102, NA19116, NA18505, NA19129, NA18511, NA07000, NA18522, NA12154
Known GenesZDHHC14
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3686e59
Frequency
Sample Size185
Observed Gain85
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer