A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507974



Internal ID22565923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73611117..73612316hg38UCSC Ensembl
chr6:74320840..74322039hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846081
Supporting Variants
Samples
Known GenesSLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507974
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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