A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702302



Internal ID15438954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44338308..44409902hg38UCSC Ensembl
Innerchr7:44377907..44449501hg19UCSC Ensembl
Innerchr7:44344432..44416026hg18UCSC Ensembl
Innerchr7:44151147..44222741hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3871595
hg1971595
hg1871595
hg1771595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526063
Supporting Variants
Samples
Known GenesNUDCD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702302
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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