A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321362



Internal ID20854467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10356972..10379069hg38UCSC Ensembl
chr1:10417030..10439127hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3822098
hg1922098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050224
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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