A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178431



Internal ID20745471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48901842..48909259hg38UCSC Ensembl
chr12:49295625..49303042hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg387418
hg197418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468809
Supporting Variants
Samples
Known GenesCCDC65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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