A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683655



Internal ID15073621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143391730..143400007hg38UCSC Ensembl
Innerchr7:143088823..143097100hg19UCSC Ensembl
Innerchr7:142798945..142807222hg18UCSC Ensembl
Innerchr7:142605660..142613937hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg388278
hg198278
hg188278
hg178278
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517520
Supporting Variants
Samples
Known GenesEPHA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683655
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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