A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656514



Internal ID18954795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76445651..76671318hg38UCSC Ensembl
Innerchr7:76074968..76300635hg19UCSC Ensembl
Innerchr7:75912904..76138571hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38225668
hg19225668
hg18225668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021715
Supporting Variants
Samples
Known GenesDTX2, FDPSP2, LOC100133091, 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)nssv3656514
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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