A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430723



Internal ID22488593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51861120..51861120hg38UCSC Ensembl
chr7:51928816..51928816hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430723
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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