A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643632



Internal ID7030391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9304825..9315673hg38UCSC Ensembl
chr19:9415501..9426349hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810849
hg1910849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15990167, essv15990166, essv15990168
SamplesNA12751, HG02620, NA18853
Known GenesZNF699
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643632
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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