A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436614



Internal ID21094167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26380764..26521081hg38UCSC Ensembl
chr10:26669693..26810010hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38140318
hg19140318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189358
Samples
Known GenesAPBB1IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436614
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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