A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654300



Internal ID15390952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154906001..154909643hg38UCSC Ensembl
Innerchr7:154697711..154701353hg19UCSC Ensembl
Innerchr7:154328644..154332286hg18UCSC Ensembl
Innerchr7:154135359..154139001hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg383643
hg193643
hg183643
hg173643
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517537
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654300
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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