A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1156n54



Internal ID20134580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54476971..54513792hg38UCSC Ensembl
chr10:56236731..56273552hg19UCSC Ensembl
chr10:55906737..55943558hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3836822
hg1936822
hg1836822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550958, nsv550961
SamplesHGDP01263, 1782681093_A
Known GenesPCDH15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1156n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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