A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355810



Internal ID21013363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3302406..3305489hg38UCSC Ensembl
chr4:3304133..3307216hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383084
hg193084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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