A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv962n54



Internal ID22768857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14933172..15031994hg38UCSC Ensembl
chr10:14975171..15073993hg19UCSC Ensembl
chr10:15015177..15113999hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3898823
hg1998823
hg1898823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550005, nsv550008, nsv550009, nsv550010, nsv550004, nsv550002
SamplesHGDP00475, NINDS_174, HGDP00072, HGDP00464, HGDP00647
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv962n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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