A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438840



Internal ID22496710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130080159..130080584hg38UCSC Ensembl
chr9:132842438..132842863hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907758
Supporting Variants
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438840
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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