A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1090220



Internal ID15943406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93443009..93553245hg38UCSC Ensembl
Innerchr7:93072321..93182557hg19UCSC Ensembl
Innerchr7:92910257..93020493hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38110237
hg19110237
hg18110237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607815
Supporting Variants
Samples
Known GenesCALCR, MIR489, MIR653
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1090220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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