A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5605047



Internal ID9621515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36417132..36423544hg38UCSC Ensembl
Outerchr6:36417095..36423594hg38UCSC Ensembl
Innerchr6:36384909..36391321hg19UCSC Ensembl
Outerchr6:36384872..36391371hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671959
Supporting Variants
SamplesNA19331
Known GenesPXT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5605047
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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