A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449525



Internal ID21107078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58916652..58918394hg38UCSC Ensembl
chr10:60676412..60678154hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381743
hg191743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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