A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8985n54



Internal ID22776880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25552889..25581859hg38UCSC Ensembl
chr4:25554511..25583481hg19UCSC Ensembl
chr4:25163609..25192579hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3828971
hg1928971
hg1828971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593837, nsv593829, nsv593836, nsv593833, nsv593832, nsv593831, nsv593834
SamplesHGDP01385, 1780854518_A, HGDP00154, HGDP00023, HGDP00226, 1782681110_A, HGDP00205, HGDP00144, 1780862575_A, HGDP00035, NINDS_95, HGDP00602, 1780862577_A, HGDP00740, HGDP01153, HGDP00011, HGDP00125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8985n54
Frequency
Sample Size17421
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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