A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506396



Internal ID20879675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39739172..39739762hg38UCSC Ensembl
chr15:40031373..40031963hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024185
Samples
Known GenesFSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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