A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5678144



Internal ID9517457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107256285..107258391hg38UCSC Ensembl
Outerchr9:107255914..107258761hg38UCSC Ensembl
Innerchr9:110018566..110020672hg19UCSC Ensembl
Outerchr9:110018195..110021042hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661196
Supporting Variants
SamplesNA19004
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5678144
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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