A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322423



Internal ID20855536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45642535..45652146hg38UCSC Ensembl
chr1:46108207..46117818hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg389612
hg199612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061098
Samples
Known GenesGPBP1L1, RPS15AP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322423
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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