A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507009



Internal ID20880297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95459324..95459906hg38UCSC Ensembl
chr15:96002553..96003135hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027143
Samples
Known GenesLINC00924
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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