A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694912



Internal ID15431564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22877281..23000391hg38UCSC Ensembl
Innerchr4:22878904..23002014hg19UCSC Ensembl
Innerchr4:22488002..22611112hg18UCSC Ensembl
Innerchr4:22555173..22678283hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38123111
hg19123111
hg18123111
hg17123111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522138
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694912
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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