A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687745



Internal ID15077711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143095565..143155721hg38UCSC Ensembl
Innerchr7:142792658..142852814hg19UCSC Ensembl
Innerchr7:142502780..142562936hg18UCSC Ensembl
Innerchr7:142309495..142369651hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3860157
hg1960157
hg1860157
hg1760157
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516782
Supporting Variants
Samples
Known GenesPIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687745
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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