A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611714



Internal ID6998619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169475183..169486070hg38UCSC Ensembl
Innerchr6:169475184..169486069hg38UCSC Ensembl
Outerchr6:169475182..169486071hg38UCSC Ensembl
chr6:169875278..169886165hg19UCSC Ensembl
Innerchr6:169875279..169886164hg19UCSC Ensembl
Outerchr6:169875277..169886166hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810888
hg1910888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12649161
SamplesHG02271
Known GenesWDR27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611714
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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