A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705491



Internal ID15095457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56267672..56274039hg38UCSC Ensembl
Innerchr19:56779041..56785408hg19UCSC Ensembl
Innerchr19:61470853..61477220hg18UCSC Ensembl
Innerchr19:61470853..61477220hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg386368
hg196368
hg186368
hg176368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528817
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705491
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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