A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495793



Internal ID20868988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92648090..92648525hg38UCSC Ensembl
chr15:93191320..93191755hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027307
Samples
Known GenesFAM174B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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