A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612567



Internal ID6999467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24194410..24201159hg38UCSC Ensembl
chr7:24234029..24240778hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386750
hg196750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12706703, essv12706704
SamplesNA19678, NA20821
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612567
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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