A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138655



Internal ID21507776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39334571..39334697hg38UCSC Ensembl
chr5:39334673..39334799hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575380
Supporting Variants
SamplesNA20509
Known GenesC9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138655
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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