A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506625



Internal ID20879908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48916596..48917383hg38UCSC Ensembl
chr15:49208793..49209580hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024754
Samples
Known GenesSHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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