A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501290



Internal ID22559228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133139945..133141244hg38UCSC Ensembl
chr7:132824704..132826003hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501290
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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