A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435268



Internal ID22493138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79468045..79468095hg38UCSC Ensembl
chr7:79097361..79097411hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907959
Supporting Variants
Samples
Known GenesMAGI2-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435268
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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