A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853950



Internal ID22628885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24568784..24575806hg38UCSC Ensembl
chr14:25037990..25045012hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg387023
hg197023
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456461
Samples
Known GenesCTSG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853950
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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