A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500963



Internal ID22558900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116137216..116138615hg38UCSC Ensembl
chr6:116458379..116459778hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844230
Supporting Variants
Samples
Known GenesNT5DC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500963
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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