A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12686007



Internal ID2836358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15210337..15284647hg38UCSC Ensembl
chr7:15249962..15324272hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3874311
hg1974311
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612352
Supporting Variants
SamplesHG02501
Known GenesAGMO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12686007
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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