A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615009



Internal ID7001898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129957057..129963176hg38UCSC Ensembl
Innerchr7:129957557..129962676hg38UCSC Ensembl
Outerchr7:129956057..129964176hg38UCSC Ensembl
chr7:129596897..129603016hg19UCSC Ensembl
Innerchr7:129597397..129602516hg19UCSC Ensembl
Outerchr7:129595897..129604016hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg386120
hg196120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12971706
SamplesHG03693
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615009
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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