A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663571



Internal ID9929676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121570801..121576509hg38UCSC Ensembl
Outerchr9:121570764..121576559hg38UCSC Ensembl
Innerchr9:124333080..124338788hg19UCSC Ensembl
Outerchr9:124333043..124338838hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385796
hg195796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6577172
SamplesNA19236
Known GenesDAB2IP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663571
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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