A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6566n54



Internal ID20139990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54748501..54776074hg38UCSC Ensembl
chr19:55259953..55287526hg19UCSC Ensembl
chr19:59951765..59979338hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3827574
hg1927574
hg1827574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580264, nsv580256, nsv580262, nsv580265, nsv580257, nsv580266, nsv580268, nsv580263
Samples
Known GenesKIR2DL1, KIR2DL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6566n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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