A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435192



Internal ID22493062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127464362..127464417hg38UCSC Ensembl
chr9:130226641..130226696hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923696
Supporting Variants
Samples
Known GenesLRSAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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