A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705662



Internal ID15095628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:244417046..244426450hg38UCSC Ensembl
Innerchr1:244580348..244589752hg19UCSC Ensembl
Innerchr1:242646971..242656375hg18UCSC Ensembl
Innerchr1:240906389..240915793hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg389405
hg199405
hg189405
hg179405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516557
Supporting Variants
Samples
Known GenesADSS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705662
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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