A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474893



Internal ID22532788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90497680..90499019hg38UCSC Ensembl
chr15:91040912..91042251hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381340
hg191340
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870446
Supporting Variants
Samples
Known GenesIQGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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