A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890744



Internal ID18838360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140846323..140853802hg38UCSC Ensembl
Outerchr5:140846323..140857963hg38UCSC Ensembl
Innerchr5:140225908..140233387hg19UCSC Ensembl
Outerchr5:140225908..140237548hg19UCSC Ensembl
Innerchr5:140206092..140213571hg18UCSC Ensembl
Outerchr5:140206092..140217732hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3811641
hg1911641
hg1811641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796674, essv25796232, essv25796528, essv25797467
Samples
Known GenesPCDHA1, PCDHA10, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890744
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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