A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998167



Internal ID66324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76071507..76072766hg38UCSC Ensembl
chr7:75700825..75702084hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998167
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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