A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005140



Internal ID71052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128104960..128105057hg38UCSC Ensembl
chr7:127745012..127745109hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005140
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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