A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16002824



Internal ID6004640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16695362..16701870hg38UCSC Ensembl
Innerchr19:16695512..16701720hg38UCSC Ensembl
Outerchr19:16695212..16702020hg38UCSC Ensembl
chr19:16806173..16812681hg19UCSC Ensembl
Innerchr19:16806323..16812531hg19UCSC Ensembl
Outerchr19:16806023..16812831hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg386509
hg196509
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643801
Supporting Variants
SamplesNA20878
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16002824
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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