A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933683



Internal ID15880953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237645391..237648778hg38UCSC Ensembl
Innerchr2:238554034..238557421hg19UCSC Ensembl
Innerchr2:238218773..238222160hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg383388
hg193388
hg183388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584743
Supporting Variants
Samples
Known GenesLRRFIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933683
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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