A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15974733



Internal ID5976549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3703997..3709201hg38UCSC Ensembl
Innerchr19:3704022..3709176hg38UCSC Ensembl
Outerchr19:3703972..3709226hg38UCSC Ensembl
chr19:3703995..3709199hg19UCSC Ensembl
Innerchr19:3704020..3709174hg19UCSC Ensembl
Outerchr19:3703970..3709224hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385205
hg195205
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643466
Supporting Variants
SamplesHG00592
Known GenesTJP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15974733
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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