A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644251



Internal ID7031007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36251138..36256673hg38UCSC Ensembl
Innerchr19:36251155..36256657hg38UCSC Ensembl
Outerchr19:36251122..36256690hg38UCSC Ensembl
chr19:36742040..36747575hg19UCSC Ensembl
Innerchr19:36742057..36747559hg19UCSC Ensembl
Outerchr19:36742024..36747592hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385536
hg195536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16048767
SamplesHG03897
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644251
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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