A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612601



Internal ID6999501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25532538..25540124hg38UCSC Ensembl
Innerchr7:25532538..25540124hg38UCSC Ensembl
Outerchr7:25532417..25540270hg38UCSC Ensembl
chr7:25572158..25579744hg19UCSC Ensembl
Innerchr7:25572158..25579744hg19UCSC Ensembl
Outerchr7:25572037..25579890hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg387587
hg197587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12709422, essv12709421
SamplesNA19332, NA19374
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612601
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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