A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10278n54



Internal ID22778173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4238254..4481187hg38UCSC Ensembl
chr6:4238488..4481421hg19UCSC Ensembl
chr6:4183487..4426420hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38242934
hg19242934
hg18242934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600868, nsv600861, nsv600866, nsv600862, nsv600864, nsv600867, nsv600863, nsv600865
SamplesNINDS_147, NINDS_271
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10278n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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