A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438112



Internal ID22495982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135563240..135563335hg38UCSC Ensembl
chr9:138455086..138455181hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920002
Supporting Variants
Samples
Known GenesPAEP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438112
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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