A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703987



Internal ID15093953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141468203..141471560hg38UCSC Ensembl
Innerchr7:141168003..141171360hg19UCSC Ensembl
Innerchr7:140814472..140817829hg18UCSC Ensembl
Innerchr7:140621187..140624544hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg383358
hg193358
hg183358
hg173358
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527529
Supporting Variants
Samples
Known GenesTMEM178B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703987
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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