A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703872



Internal ID15440524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135502662..135506407hg38UCSC Ensembl
Innerchr3:135221504..135225249hg19UCSC Ensembl
Innerchr3:136704194..136707939hg18UCSC Ensembl
Innerchr3:136704202..136707947hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383746
hg193746
hg183746
hg173746
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527433
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703872
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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