A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605625



Internal ID6992563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82918896..82956696hg38UCSC Ensembl
Innerchr5:82918900..82956692hg38UCSC Ensembl
Outerchr5:82918892..82956700hg38UCSC Ensembl
chr5:82214715..82252515hg19UCSC Ensembl
Innerchr5:82214719..82252511hg19UCSC Ensembl
Outerchr5:82214711..82252519hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3837801
hg1937801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11957930
SamplesHG01269
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605625
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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