A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329230



Internal ID20862381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100470601..100472400hg38UCSC Ensembl
chr1:100936157..100937956hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049590
Samples
Known GenesCDC14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329230
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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