A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513590



Internal ID22571545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43115056..43125208hg38UCSC Ensembl
chr9:42860111..42870202hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3810153
hg1910092
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855770
Supporting Variants
Samples
Known GenesAQP7P3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513590
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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