A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471857



Internal ID22529749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43780285..43784298hg38UCSC Ensembl
chr15:44072483..44076496hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg384014
hg194014
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858297
Supporting Variants
Samples
Known GenesSERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471857
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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