A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613561



Internal ID7000457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67768737..67770044hg38UCSC Ensembl
Innerchr7:67768801..67769981hg38UCSC Ensembl
Outerchr7:67768674..67770108hg38UCSC Ensembl
chr7:67233724..67235031hg19UCSC Ensembl
Innerchr7:67233788..67234968hg19UCSC Ensembl
Outerchr7:67233661..67235095hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12826528
SamplesHG02382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613561
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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