A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088026



Internal ID15594526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76482621..76847653hg38UCSC Ensembl
Innerchr7:76111938..76476970hg19UCSC Ensembl
Innerchr7:75949874..76314906hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38365033
hg19365033
hg18365033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607587
Supporting Variants
Samples
Known GenesDTX2, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1088026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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