A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443008



Internal ID22500878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97361455..97361535hg38UCSC Ensembl
chr7:96990767..96990847hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443008
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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