A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582215



Internal ID16369624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:74498017..74505288hg38UCSC Ensembl
Innerchr2:74725144..74732415hg19UCSC Ensembl
Innerchr2:74578652..74585923hg18UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg387272
hg197272
hg187272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv912191
Samples
Known GenesLBX2, LBX2-AS1, PCGF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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