A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329588



Internal ID20862741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54912307..54925483hg38UCSC Ensembl
chr1:55377980..55391156hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3813177
hg1913177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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