A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10462n54



Internal ID20143886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31814840..31829645hg38UCSC Ensembl
chr6:31782617..31797422hg19UCSC Ensembl
chr6:31890596..31905401hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3814806
hg1914806
hg1814806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601949, nsv601952, nsv601953, nsv601948, nsv601947, nsv601957, nsv601954, nsv601946
Samples
Known GenesHSPA1A, HSPA1B, HSPA1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10462n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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