A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668562



Internal ID15405214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42704111..42706677hg38UCSC Ensembl
Innerchr4:42706128..42708694hg19UCSC Ensembl
Innerchr4:42400885..42403451hg18UCSC Ensembl
Innerchr4:42547056..42549622hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382567
hg192567
hg182567
hg172567
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515863
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668562
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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