A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329842



Internal ID20862995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32203042..32203366hg38UCSC Ensembl
chr1:32668643..32668967hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060437
Samples
Known GenesCCDC28B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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