A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1042395



Internal ID15895581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140853458..140855953hg38UCSC Ensembl
Innerchr5:140233043..140235538hg19UCSC Ensembl
Innerchr5:140213227..140215722hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382496
hg192496
hg182496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599899
Supporting Variants
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)nssv1042395
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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