A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116968



Internal ID20684008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36189699..36190281hg38UCSC Ensembl
chr4:36191321..36191903hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355714
Supporting Variants
Samples
Known GenesARAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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