A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452684



Internal ID21110237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89412101..89418800hg38UCSC Ensembl
chr10:91171858..91178557hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182675
Samples
Known GenesIFIT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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