A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436503



Internal ID21094056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37852901..37860600hg38UCSC Ensembl
chr10:38141829..38149528hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194066
Samples
Known GenesZNF248
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436503
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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