A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607585



Internal ID16048308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76436872..76813633hg38UCSC Ensembl
Innerchr7:76066189..76442950hg19UCSC Ensembl
Innerchr7:75904125..76280886hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38376762
hg19376762
hg18376762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1088024
Samples
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, UPK3B, ZP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607585
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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