A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467497



Internal ID22525388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110488347..110489481hg38UCSC Ensembl
chr1:111030969..111032103hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827708
Supporting Variants
Samples
Known GenesCYMP, LOC440602
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467497
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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