A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712042



Internal ID15659312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26352550..26370135hg38UCSC Ensembl
Innerchr1:26679041..26696626hg19UCSC Ensembl
Innerchr1:26551628..26569213hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3817586
hg1917586
hg1817586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545907
Supporting Variants
Samples
Known GenesAIM1L, ZNF683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712042
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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