A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507554



Internal ID20880847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81323376..81323958hg38UCSC Ensembl
chr15:81615717..81616299hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191731
Samples
Known GenesSTARD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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