A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1081797



Internal ID15588297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:30915752..30916814hg38UCSC Ensembl
Innerchr7:30955367..30956429hg19UCSC Ensembl
Innerchr7:30921892..30922954hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381063
hg191063
hg181063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606520
Supporting Variants
Samples
Known GenesAQP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1081797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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