A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318752



Internal ID20851844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32109775..32119833hg38UCSC Ensembl
chr1:32575376..32585434hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3810059
hg1910059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060430
Samples
Known GenesKPNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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