A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613621



Internal ID6653830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71181391..71182773hg38UCSC Ensembl
Innerchr7:71181429..71182736hg38UCSC Ensembl
Outerchr7:71181354..71182811hg38UCSC Ensembl
chr7:70646377..70647759hg19UCSC Ensembl
Innerchr7:70646415..70647722hg19UCSC Ensembl
Outerchr7:70646340..70647797hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381383
hg191383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12829415
SamplesHG02137
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613621
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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