A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318240



Internal ID20851332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64407259..64435145hg38UCSC Ensembl
chr1:64872942..64900828hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3827887
hg1927887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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