A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083177



Internal ID15936363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43585908..43604236hg38UCSC Ensembl
Innerchr7:43625507..43643835hg19UCSC Ensembl
Innerchr7:43592032..43610360hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3818329
hg1918329
hg1818329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606728
Supporting Variants
Samples
Known GenesSTK17A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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