A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328697



Internal ID20861846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16456245..16464887hg38UCSC Ensembl
chr1:16782740..16791382hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg388643
hg198643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201920
Samples
Known GenesNECAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328697
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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