A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655995



Internal ID15392647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26282850..26290933hg38UCSC Ensembl
Innerchr4:26284472..26292555hg19UCSC Ensembl
Innerchr4:25893570..25901653hg18UCSC Ensembl
Innerchr4:25960741..25968824hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388084
hg198084
hg188084
hg178084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519405
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655995
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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