A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798162



Internal ID21243500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76392842..76394307hg38UCSC Ensembl
chr18:74104798..74106263hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381466
hg191466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691526
Samples
Known GenesZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798162
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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