A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643586



Internal ID7030345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7472792..7474462hg38UCSC Ensembl
Innerchr19:7472845..7474410hg38UCSC Ensembl
Outerchr19:7472740..7474515hg38UCSC Ensembl
chr19:7537678..7539348hg19UCSC Ensembl
Innerchr19:7537731..7539296hg19UCSC Ensembl
Outerchr19:7537626..7539401hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381671
hg191671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15987328, essv15987325, essv15987319, essv15987321, essv15987324, essv15987322, essv15987320, essv15987323, essv15987327, essv15987326
SamplesNA20874, HG03773, NA21115, HG02493, HG04219, HG03695, HG03850, HG04141, NA20888, HG04015
Known GenesLOC100128573
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643586
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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