A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376276



Internal ID21033829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159532067..159613448hg38UCSC Ensembl
chr4:160453219..160534600hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3881382
hg1981382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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