A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374776



Internal ID21032329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2423581..2427872hg38UCSC Ensembl
chr4:2425308..2429599hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg384292
hg194292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113340
Samples
Known GenesLOC402160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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