A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326549



Internal ID20859685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87568864..87569067hg38UCSC Ensembl
chr1:88034547..88034750hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326549
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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