A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12843200



Internal ID889076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74211663..74213621hg38UCSC Ensembl
Innerchr7:74211713..74213571hg38UCSC Ensembl
Outerchr7:74211613..74213671hg38UCSC Ensembl
chr7:73625993..73627951hg19UCSC Ensembl
Innerchr7:73626043..73627901hg19UCSC Ensembl
Outerchr7:73625943..73628001hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381959
hg191959
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613704
Supporting Variants
SamplesHG00478
Known GenesLAT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12843200
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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