A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv156n54



Internal ID22768051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16019962..16050336hg38UCSC Ensembl
chr1:16346457..16376831hg19UCSC Ensembl
chr1:16219044..16249418hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3830375
hg1930375
hg1830375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545630, nsv545632, nsv545631
SamplesHGDP00934, HGDP00906, HGDP00941
Known GenesCLCNKA, CLCNKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv156n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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