A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495758



Internal ID20868952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99913571..100381017hg38UCSC Ensembl
chr15:100453776..100921222hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38467447
hg19467447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2649n223
Supporting Variantsnssv18186557
Samples
Known GenesADAMTS17, SPATA41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495758
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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