A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040713



Internal ID19129932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11555955..11599661hg38UCSC Ensembl
Innerchr10:11597954..11641660hg19UCSC Ensembl
Innerchr10:11637960..11681666hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3843707
hg1943707
hg1843707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486451
Samples
Known GenesUSP6NL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040713
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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