A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12903615



Internal ID6100047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97515430..97535926hg38UCSC Ensembl
Innerchr7:97515449..97535907hg38UCSC Ensembl
Outerchr7:97515411..97535945hg38UCSC Ensembl
chr7:97144742..97165238hg19UCSC Ensembl
Innerchr7:97144761..97165219hg19UCSC Ensembl
Outerchr7:97144723..97165257hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3820497
hg1920497
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614236
Supporting Variants
SamplesNA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12903615
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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