A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599862



Internal ID16040585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140849850..140856513hg38UCSC Ensembl
Innerchr5:140229435..140236098hg19UCSC Ensembl
Innerchr5:140209619..140216282hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg386664
hg196664
hg186664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10097n54
Supporting Variantsnssv1042215
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)nsv599862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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