A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444821



Internal ID22502691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1614219..1636401hg38UCSC Ensembl
chr7:1653855..1676037hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3822183
hg1922183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919155
Supporting Variants
Samples
Known GenesTFAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444821
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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