A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6269002



Internal ID9246405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159665384..159668790hg38UCSC Ensembl
Outerchr6:159665013..159669160hg38UCSC Ensembl
Innerchr6:160086416..160089822hg19UCSC Ensembl
Outerchr6:160086045..160090192hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384148
hg194148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656557
Supporting Variants
SamplesHG00180
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6269002
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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