A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632725



Internal ID7019536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74552312..74592122hg38UCSC Ensembl
Innerchr13:74552333..74592102hg38UCSC Ensembl
Outerchr13:74552292..74592143hg38UCSC Ensembl
chr13:75126449..75166259hg19UCSC Ensembl
Innerchr13:75126470..75166239hg19UCSC Ensembl
Outerchr13:75126429..75166280hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3839811
hg1939811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14796533
SamplesHG02724
Known GenesLINC00347
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632725
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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