A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16033396



Internal ID6035212
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644138
Supporting Variants
SamplesHG03802
Known GenesZNF536
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16033396
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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