A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332341



Internal ID20865511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24456603..24461672hg38UCSC Ensembl
chr1:24783093..24788162hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385070
hg195070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059651
Samples
Known GenesNIPAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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