A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644138



Internal ID6684206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30459146..30461529hg38UCSC Ensembl
Innerchr19:30459196..30461479hg38UCSC Ensembl
Outerchr19:30459096..30461579hg38UCSC Ensembl
chr19:30950053..30952436hg19UCSC Ensembl
Innerchr19:30950103..30952386hg19UCSC Ensembl
Outerchr19:30950003..30952486hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg382384
hg192384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16033396, essv16033395
SamplesHG03802, HG03730
Known GenesZNF536
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644138
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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