A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335512



Internal ID20868704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64135089..64135510hg38UCSC Ensembl
chr1:64600772..64601193hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062358
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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