A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv155n54



Internal ID22768050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16013965..16066862hg38UCSC Ensembl
chr1:16340460..16393357hg19UCSC Ensembl
chr1:16213047..16265944hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3852898
hg1952898
hg1852898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545633, nsv545629
SamplesHGDP01090, HGDP00923
Known GenesCLCNKA, CLCNKB, FAM131C, HSPB7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv155n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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