A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439592



Internal ID22497462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126665228..126665538hg38UCSC Ensembl
chr9:129427507..129427817hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907703
Supporting Variants
Samples
Known GenesLMX1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439592
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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