A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324744



Internal ID20857872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168773327..168774217hg38UCSC Ensembl
chr1:168742565..168743455hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324744
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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