A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434903



Internal ID22492773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15603675..15603740hg38UCSC Ensembl
chr9:15603673..15603738hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923367
Supporting Variants
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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