A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444339



Internal ID22502209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55342168..55342412hg38UCSC Ensembl
chr7:55409861..55410105hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444339
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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