A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444349



Internal ID22502219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131523665..131532455hg38UCSC Ensembl
chr7:131208424..131217214hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg388791
hg198791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919047
Supporting Variants
Samples
Known GenesPODXL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444349
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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