A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441037



Internal ID21098590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97708197..97717575hg38UCSC Ensembl
chr10:99467954..99477332hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg389379
hg199379
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183320
Samples
Known GenesMARVELD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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