A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327583



Internal ID20860723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21789501..21795500hg38UCSC Ensembl
chr1:22115994..22121993hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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