A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706105



Internal ID15442757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104380525..104380580hg38UCSC Ensembl
Innerchr7:104020973..104021028hg19UCSC Ensembl
Innerchr7:103808209..103808264hg18UCSC Ensembl
Innerchr7:103614924..103614979hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
hg1756
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522695
Supporting Variants
Samples
Known GenesLHFPL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706105
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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