A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703815



Internal ID15093781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16015985..16016991hg38UCSC Ensembl
Innerchr19:16126795..16127801hg19UCSC Ensembl
Innerchr19:15987795..15988801hg18UCSC Ensembl
Innerchr19:15987795..15988801hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381007
hg191007
hg181007
hg171007
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517514
Supporting Variants
Samples
Known GenesLINC00661
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703815
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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