A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1965n54



Internal ID20135389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64566642..64806117hg38UCSC Ensembl
chr11:64334114..64573589hg19UCSC Ensembl
chr11:64090690..64330165hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38239476
hg19239476
hg18239476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555196, nsv555198, nsv555195
Samples
Known GenesMAP4K2, MEN1, NRXN2, PYGM, RASGRP2, SF1, SLC22A11, SLC22A12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1965n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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