A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994983



Internal ID64087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26579867..26590827hg38UCSC Ensembl
chr7:26619486..26630446hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3810961
hg1910961
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560175
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994983
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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