A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330256



Internal ID20863412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16003139..16004713hg38UCSC Ensembl
chr1:16329634..16331208hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052440
Samples
Known GenesC1orf64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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