A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611113



Internal ID6998024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144578406..144580017hg38UCSC Ensembl
Innerchr6:144578423..144580000hg38UCSC Ensembl
Outerchr6:144578389..144580034hg38UCSC Ensembl
chr6:144899542..144901153hg19UCSC Ensembl
Innerchr6:144899559..144901136hg19UCSC Ensembl
Outerchr6:144899525..144901170hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381612
hg191612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12576169
SamplesHG02082
Known GenesUTRN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611113
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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