A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444284



Internal ID22502154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23445412..23445496hg38UCSC Ensembl
chr7:23485031..23485115hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909012
Supporting Variants
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444284
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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