A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2940881



Internal ID15410186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143526465..143843910hg38UCSC Ensembl
Innerchr7:143223558..143541003hg19UCSC Ensembl
Innerchr7:142933680..143171936hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38317446
hg19317446
hg18238257
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514455
Supporting Variants
SamplesNA19190
Known GenesCTAGE15, CTAGE6, FAM115C, LOC154761
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2940881
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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