A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705787



Internal ID15095753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226235871..226268233hg38UCSC Ensembl
Innerchr1:226423572..226455934hg19UCSC Ensembl
Innerchr1:224490195..224522557hg18UCSC Ensembl
Innerchr1:222730307..222762669hg17UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3832363
hg1932363
hg1832363
hg1732363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517107
Supporting Variants
Samples
Known GenesLIN9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705787
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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