A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501969



Internal ID20875209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85407701..85410900hg38UCSC Ensembl
chr15:85950932..85954131hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026711
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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