A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10957n54



Internal ID22778852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143867668..143878279hg38UCSC Ensembl
chr6:144188805..144199416hg19UCSC Ensembl
chr6:144230498..144241109hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3810612
hg1910612
hg1810612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604807, nsv604806
Samples
Known GenesZC2HC1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10957n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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