A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848601



Internal ID22623536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43727291..43743597hg38UCSC Ensembl
chr15:44019489..44035795hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3816307
hg1916307
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471640
Samples
Known GenesCATSPER2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848601
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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