A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6097124



Internal ID9074527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:247022929..247023819hg38UCSC Ensembl
chr1:247186231..247187121hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673254
Supporting Variants
SamplesNA19462
Known GenesZNF670-ZNF695
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6097124
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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