A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15990181



Internal ID820656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9658008..9660519hg38UCSC Ensembl
Innerchr19:9658023..9660505hg38UCSC Ensembl
Outerchr19:9657994..9660534hg38UCSC Ensembl
chr19:9768684..9771195hg19UCSC Ensembl
Innerchr19:9768699..9771181hg19UCSC Ensembl
Outerchr19:9768670..9771210hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382512
hg192512
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643639
Supporting Variants
SamplesHG00407
Known GenesZNF562
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15990181
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer