A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005320



Internal ID19094537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110827750..110852244hg38UCSC Ensembl
Innerchr1:111370372..111394866hg19UCSC Ensembl
Innerchr1:111171895..111196389hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3824495
hg1924495
hg1824495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3490529
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)nsv1005320
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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