A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652261



Internal ID15042227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143382713..143400007hg38UCSC Ensembl
Innerchr7:143079806..143097100hg19UCSC Ensembl
Innerchr7:142789928..142807222hg18UCSC Ensembl
Innerchr7:142596643..142613937hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3817295
hg1917295
hg1817295
hg1717295
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517520
Supporting Variants
Samples
Known GenesEPHA1, MIR6892, ZYX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652261
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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