A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698184



Internal ID15088150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201891498..201919841hg38UCSC Ensembl
Innerchr1:201860626..201888969hg19UCSC Ensembl
Innerchr1:200127249..200155592hg18UCSC Ensembl
Innerchr1:198592283..198620626hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3828344
hg1928344
hg1828344
hg1728344
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521567
Supporting Variants
Samples
Known GenesLMOD1, SHISA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698184
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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