A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380932



Internal ID21038485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70636434..70639720hg38UCSC Ensembl
chr4:71502151..71505437hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg383287
hg193287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211721
Samples
Known GenesENAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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