A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707700



Internal ID19005981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19126646..19538355hg38UCSC Ensembl
Innerchr10:19415575..19827284hg19UCSC Ensembl
Innerchr10:19455581..19867290hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38411710
hg19411710
hg18411710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043780
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)nssv3707700
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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