A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999021



Internal ID66914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87351527..87351578hg38UCSC Ensembl
chr7:86980843..86980894hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405418
Supporting Variants
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999021
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006612


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