A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478785



Internal ID22536687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45600220..45630941hg38UCSC Ensembl
chr17:43677586..43708307hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3830722
hg1930722
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880154
Supporting Variants
Samples
Known GenesCRHR1, LOC644172, MGC57346
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478785
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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