A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091886



Internal ID15598386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101160859..101230554hg38UCSC Ensembl
Innerchr7:100804140..100873835hg19UCSC Ensembl
Innerchr7:100590860..100660555hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3869696
hg1969696
hg1869696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607975
Supporting Variants
Samples
Known GenesAP1S1, MOGAT3, NAT16, PLOD3, VGF, ZNHIT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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