A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591053



Internal ID6631337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63313527..63338048hg38UCSC Ensembl
Innerchr2:63313535..63338040hg38UCSC Ensembl
Outerchr2:63313519..63338056hg38UCSC Ensembl
chr2:63540662..63565183hg19UCSC Ensembl
Innerchr2:63540670..63565175hg19UCSC Ensembl
Outerchr2:63540654..63565191hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3824522
hg1924522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10522188, essv10522189
SamplesHG02379, HG00671
Known GenesWDPCP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591053
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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