A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760501



Internal ID19058782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36566134..36622783hg38UCSC Ensembl
Innerchr8:36423652..36480301hg19UCSC Ensembl
Innerchr8:36542810..36599459hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3856650
hg1956650
hg1856650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016306
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760501
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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