A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328488



Internal ID20861636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21618301..21619500hg38UCSC Ensembl
chr1:21944794..21945993hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057282
Samples
Known GenesRAP1GAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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