A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471878



Internal ID22529770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44524067..44526316hg38UCSC Ensembl
chr15:44816265..44818514hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849723
Supporting Variants
Samples
Known GenesCTDSPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471878
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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