A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061601



Internal ID21432579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17358269..17358590hg38UCSC Ensembl
chr1:17684764..17685085hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576067
Supporting Variants
SamplesHG00731
Known GenesPADI4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061601
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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