A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6577172



Internal ID9599462
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 Flag1
Merged StatusS
Merged Variantsesv2663571
Supporting Variants
SamplesNA19236
Known GenesDAB2IP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6577172
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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