A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610086



Internal ID6997005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97247775..97261469hg38UCSC Ensembl
chr6:97695651..97709345hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3813695
hg1913695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12473315
SamplesHG03920
Known GenesMIR548H3, MMS22L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610086
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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