A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448237



Internal ID22506107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44629500..44629759hg38UCSC Ensembl
chr7:44669099..44669358hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919936
Supporting Variants
Samples
Known GenesOGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448237
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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