A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599894



Internal ID16040617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140852761..140864165hg38UCSC Ensembl
Innerchr5:140232346..140243750hg19UCSC Ensembl
Innerchr5:140212530..140223934hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3811405
hg1911405
hg1811405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1042384
Samples
Known GenesPCDHA1, PCDHA10, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599894
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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