A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6069574



Internal ID9049910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91879739..91883681hg38UCSC Ensembl
Outerchr6:91879582..91883834hg38UCSC Ensembl
Innerchr6:92589457..92593399hg19UCSC Ensembl
Outerchr6:92589300..92593552hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384253
hg194253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665645
Supporting Variants
SamplesHG00693
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6069574
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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