A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12826528



Internal ID2691069
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613561
Supporting Variants
SamplesHG02382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12826528
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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