A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513499



Internal ID20886844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41313417..41473126hg38UCSC Ensembl
chr15:41605615..41765324hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38159710
hg19159710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2504n223
Supporting Variantsnssv18194955
Samples
Known GenesNDUFAF1, NUSAP1, OIP5, RTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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