A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664571



Internal ID9930676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38035805..38039389hg38UCSC Ensembl
Outerchr9:38035648..38039542hg38UCSC Ensembl
Innerchr9:38035802..38039386hg19UCSC Ensembl
Outerchr9:38035645..38039539hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383895
hg193895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6032944
SamplesNA19436
Known GenesSHB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664571
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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