A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705002



Internal ID15441654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80481620..80490226hg38UCSC Ensembl
Innerchr4:81402774..81411380hg19UCSC Ensembl
Innerchr4:81621798..81630404hg18UCSC Ensembl
Innerchr4:81759953..81768559hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg388607
hg198607
hg188607
hg178607
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528410
Supporting Variants
Samples
Known GenesC4orf22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705002
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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