A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331995



Internal ID20865164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157828430..157917737hg38UCSC Ensembl
chr1:157798220..157887527hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3889308
hg1989308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052718
Samples
Known GenesCD5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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