A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412569



Internal ID22470439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101001604..101004105hg38UCSC Ensembl
chr6:101449480..101451981hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412569
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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