A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433247



Internal ID22491117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44580306..44580775hg38UCSC Ensembl
chr7:44619905..44620374hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911634
Supporting Variants
Samples
Known GenesTMED4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433247
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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