A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507872



Internal ID20881168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80810484..80814165hg38UCSC Ensembl
chr15:81102825..81106506hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383682
hg193682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184431
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507872
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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