A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509121



Internal ID20882427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100033319..100421660hg38UCSC Ensembl
chr15:100573524..100961865hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38388342
hg19388342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186695
Samples
Known GenesADAMTS17, CERS3, SPATA41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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