A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326923



Internal ID20860060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17455912..17458236hg38UCSC Ensembl
chr1:17782408..17784732hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg382325
hg192325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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