A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002772



Internal ID19091989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:218683402..218825530hg38UCSC Ensembl
Innerchr1:218856744..218998872hg19UCSC Ensembl
Innerchr1:216923367..217065495hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38142129
hg19142129
hg18142129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3484822
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)nsv1002772
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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