A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6295610



Internal ID8876605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131369189..131373790hg38UCSC Ensembl
Outerchr9:131369152..131373840hg38UCSC Ensembl
Innerchr9:134244576..134249177hg19UCSC Ensembl
Outerchr9:134244539..134249227hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384689
hg194689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666150
Supporting Variants
SamplesHG00328
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6295610
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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