A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033529



Internal ID18776062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76506401..76661915hg38UCSC Ensembl
Innerchr7:76135718..76291232hg19UCSC Ensembl
Innerchr7:75973654..76129168hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38155515
hg19155515
hg18155515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6477n100
Supporting Variantsnssv3656531
Samples
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033529
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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