A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1087717



Internal ID15940903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75058099..75064918hg38UCSC Ensembl
Innerchr7:74473256..74480731hg19UCSC Ensembl
Innerchr7:74111192..74118667hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386820
hg197476
hg187476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607498
Supporting Variants
Samples
Known GenesWBSCR16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1087717
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