A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091885



Internal ID15598385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101149529..101328323hg38UCSC Ensembl
Innerchr7:100792810..100971604hg19UCSC Ensembl
Innerchr7:100579530..100758324hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38178795
hg19178795
hg18178795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607974
Supporting Variants
Samples
Known GenesAP1S1, CLDN15, FIS1, MIR4653, MOGAT3, NAT16, PLOD3, RABL5, VGF, ZNHIT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091885
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