A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644873



Internal ID7031624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56661100..56671569hg38UCSC Ensembl
chr19:57172468..57182937hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3810470
hg1910470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16103294, essv16103297, essv16103298, essv16103293, essv16103295, essv16103296, essv16103292
SamplesNA20762, NA20317, HG02620, NA20757, NA20318, NA19077, HG03571
Known GenesZNF835
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644873
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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