A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3486451



Internal ID19074092
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 StatusS
Merged Variantsnsv1040713
Supporting Variants
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)nssv3486451
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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