A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472938



Internal ID22530830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58146629..58149685hg38UCSC Ensembl
chr15:58438828..58441884hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383057
hg193057
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853922
Supporting Variants
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472938
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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