A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3773070



Internal ID18958563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3717730..3717782hg38UCSC Ensembl
chr6:3717964..3718016hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073953
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3773070
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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