A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612814



Internal ID6999714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35506243..35511171hg38UCSC Ensembl
Innerchr7:35506243..35511171hg38UCSC Ensembl
Outerchr7:35506128..35511316hg38UCSC Ensembl
chr7:35545853..35550781hg19UCSC Ensembl
Innerchr7:35545853..35550781hg19UCSC Ensembl
Outerchr7:35545738..35550926hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg384929
hg194929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12729535
SamplesHG00443
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612814
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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