A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436273



Internal ID22494143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144851578..144851578hg38UCSC Ensembl
chr7:144548671..144548671hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436273
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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