A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12706635



Internal ID5981487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24057529..24075323hg38UCSC Ensembl
Innerchr7:24057679..24075173hg38UCSC Ensembl
Outerchr7:24057379..24075473hg38UCSC Ensembl
chr7:24097148..24114942hg19UCSC Ensembl
Innerchr7:24097298..24114792hg19UCSC Ensembl
Outerchr7:24096998..24115092hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817795
hg1917795
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612562
Supporting Variants
SamplesNA19390
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12706635
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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