A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662046



Internal ID15398698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56691556..56703805hg38UCSC Ensembl
Innerchr19:57202924..57215173hg19UCSC Ensembl
Innerchr19:61894736..61906985hg18UCSC Ensembl
Innerchr19:61894736..61906985hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3812250
hg1912250
hg1812250
hg1712250
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517449
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662046
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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