A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3471675



Internal ID19064574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:74902800..74929721hg38UCSC Ensembl
Innerchr1:75368484..75395405hg19UCSC Ensembl
Innerchr1:75141072..75167993hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3826922
hg1926922
hg1826922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011649
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)nssv3471675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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