A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441288



Internal ID22499158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139325990..139326054hg38UCSC Ensembl
chr7:139010736..139010800hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441288
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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