A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088462



Internal ID15594962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76516684..76885926hg38UCSC Ensembl
Innerchr7:76146001..76515243hg19UCSC Ensembl
Innerchr7:75983937..76353179hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38369243
hg19369243
hg18369243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607616
Supporting Variants
Samples
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1088462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer