A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445258



Internal ID21102811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58821901..58822900hg38UCSC Ensembl
chr10:60581661..60582660hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983169
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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