A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643577



Internal ID6683648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7066680..7107642hg38UCSC Ensembl
chr19:7066691..7107653hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3840963
hg1940963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15986904, essv15986903, essv15986906, essv15986905
SamplesNA21110, HG04186, NA20524, HG04195
Known GenesZNF557
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643577
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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