A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635566



Internal ID7022365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102693271..102693793hg38UCSC Ensembl
Innerchr14:102693271..102693793hg38UCSC Ensembl
Outerchr14:102693105..102693957hg38UCSC Ensembl
chr14:103159608..103160130hg19UCSC Ensembl
Innerchr14:103159608..103160130hg19UCSC Ensembl
Outerchr14:103159442..103160294hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109976, essv15109975, essv15109979, essv15109982, essv15109977, essv15109981, essv15109984, essv15109978, essv15109980, essv15109983
SamplesHG00231, HG01465, NA19038, NA19041, NA20800, HG00266, HG00183, NA12272, HG01272, NA12776
Known GenesRCOR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635566
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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