A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560224



Internal ID16347633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112570529..112574905hg38UCSC Ensembl
Innerchr12:113008333..113012709hg19UCSC Ensembl
Innerchr12:111492716..111497092hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg384377
hg194377
hg184377
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2876n54
Supporting Variantsnssv802348, nssv802351, nssv802347, nssv802349, nssv802346, nssv802345, nssv802350
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560224
Frequency
Sample Size17421
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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