A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607919



Internal ID16395328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98391899..98495542hg38UCSC Ensembl
Innerchr7:98021211..98124854hg19UCSC Ensembl
Innerchr7:97859147..97962790hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38103644
hg19103644
hg18103644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1091635
Samples
Known GenesBAIAP2L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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