A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611799



Internal ID6998702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1027683..1039095hg38UCSC Ensembl
Innerchr7:1027683..1039095hg38UCSC Ensembl
Outerchr7:1027475..1039268hg38UCSC Ensembl
chr7:1067319..1078731hg19UCSC Ensembl
Innerchr7:1067319..1078731hg19UCSC Ensembl
Outerchr7:1067111..1078904hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3811413
hg1911413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12662085
SamplesHG01863
Known GenesC7orf50
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611799
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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