A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315916



Internal ID20848991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152756118..152761248hg38UCSC Ensembl
chr1:152728594..152733724hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg385131
hg195131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052376
Samples
Known GenesKPRP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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