A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329401



Internal ID20862553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63922497..63924022hg38UCSC Ensembl
chr1:64388168..64389693hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381526
hg191526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062341
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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