A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008763



Internal ID19097981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76226372..76257732hg38UCSC Ensembl
Innerchr1:76692057..76723417hg19UCSC Ensembl
Innerchr1:76464645..76496005hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3831361
hg1931361
hg1831361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv197n100
Supporting Variantsnssv3482237
Samples
Known GenesST6GALNAC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008763
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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