A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088028



Internal ID15594528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76502756..76516684hg38UCSC Ensembl
Innerchr7:76132073..76146001hg19UCSC Ensembl
Innerchr7:75970009..75983937hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3813929
hg1913929
hg1813929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607589
Supporting Variants
Samples
Known GenesDTX2, UPK3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1088028
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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