A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644242



Internal ID6684310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35708570..35716313hg38UCSC Ensembl
chr19:36199472..36207215hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg387744
hg197744
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16046276, essv16046273, essv16046272, essv16046274, essv16046275
SamplesHG00244, HG02153, HG03212, NA12872, HG01951
Known GenesZBTB32
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644242
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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