A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456461



Internal ID22514339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24568784..24575806hg38UCSC Ensembl
chr14:25037990..25045012hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg387023
hg197023
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853950
Supporting Variants
Samples
Known GenesCTSG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456461
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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