A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316029



Internal ID20849105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14636334..14638308hg38UCSC Ensembl
chr1:14962830..14964804hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381975
hg191975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052146
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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