A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513176



Internal ID20886517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85697411..85702017hg38UCSC Ensembl
chr15:86240642..86245248hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384607
hg194607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026724
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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