A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16103295



Internal ID6375410
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644873
Supporting Variants
SamplesNA20317
Known GenesZNF835
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16103295
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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