A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6336258



Internal ID9313661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127870950..127871763hg38UCSC Ensembl
Outerchr9:127870793..127871916hg38UCSC Ensembl
Innerchr9:130633229..130634042hg19UCSC Ensembl
Outerchr9:130633072..130634195hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669245
Supporting Variants
SamplesHG01334
Known GenesAK1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6336258
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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