A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643770



Internal ID7030528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15553571..15566313hg38UCSC Ensembl
Innerchr19:15553581..15566303hg38UCSC Ensembl
Outerchr19:15553561..15566323hg38UCSC Ensembl
chr19:15664382..15677124hg19UCSC Ensembl
Innerchr19:15664392..15677114hg19UCSC Ensembl
Outerchr19:15664372..15677134hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3812743
hg1912743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15999977, essv15999972, essv15999978, essv15999974, essv15999973, essv15999979, essv15999976, essv15999975
SamplesHG03105, NA19917, HG01176, NA19189, HG03301, HG02722, NA19144, NA19143
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643770
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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