A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116340



Internal ID20683380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40979917..40991246hg38UCSC Ensembl
chr4:40981934..40993263hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3811330
hg1911330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390634
Supporting Variants
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116340
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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