A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6066630



Internal ID9044033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127419537..127424443hg38UCSC Ensembl
Outerchr9:127419166..127424813hg38UCSC Ensembl
Innerchr9:130181816..130186722hg19UCSC Ensembl
Outerchr9:130181445..130187092hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385648
hg195648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667187
Supporting Variants
SamplesNA18560
Known GenesZNF79
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6066630
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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