A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698363



Internal ID15435015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165937582..165939551hg38UCSC Ensembl
Innerchr1:165906819..165908788hg19UCSC Ensembl
Innerchr1:164173443..164175412hg18UCSC Ensembl
Innerchr1:162638477..162640446hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381970
hg191970
hg181970
hg171970
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520206
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698363
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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