A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391122



Internal ID21048675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37447916..37459206hg38UCSC Ensembl
chr4:37449538..37460828hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3811291
hg1911291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115958
Samples
Known GenesC4orf19, KIAA1239
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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