A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705842



Internal ID15442494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55472876..55475269hg38UCSC Ensembl
Innerchr8:56385436..56387829hg19UCSC Ensembl
Innerchr8:56547990..56550383hg18UCSC Ensembl
Innerchr8:56547990..56550383hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg382394
hg192394
hg182394
hg172394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516136
Supporting Variants
Samples
Known GenesXKR4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705842
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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