A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327472



Internal ID20860611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46538221..46605477hg38UCSC Ensembl
chr1:47003893..47071149hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3867257
hg1967257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061566
Samples
Known GenesKNCN, MKNK1, MKNK1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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