A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12270952



Internal ID1986198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32526365..32526707hg38UCSC Ensembl
Innerchr6:32526415..32526657hg38UCSC Ensembl
Outerchr6:32526239..32526833hg38UCSC Ensembl
chr6:32494142..32494484hg19UCSC Ensembl
Innerchr6:32494192..32494434hg19UCSC Ensembl
Outerchr6:32494016..32494610hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608588
Supporting Variants
SamplesHG01845
Known GenesHLA-DRB5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12270952
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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