A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136809



Internal ID21414324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181326571..181326667hg38UCSC Ensembl
chr5:180753572..180753668hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579346
Supporting Variants
SamplesHG00513
Known GenesLOC100132062, LOC100132287, LOC100133331
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136809
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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