A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012077



Internal ID19101295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:195508421..195600484hg38UCSC Ensembl
Innerchr1:195477551..195569614hg19UCSC Ensembl
Innerchr1:193744174..193836237hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3892064
hg1992064
hg1892064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704874
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)nsv1012077
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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