A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443471



Internal ID21101024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91406301..91410200hg38UCSC Ensembl
chr10:93166058..93169957hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192045
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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