A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061602



Internal ID21457493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173613562..173613562hg38UCSC Ensembl
chr1:173582701..173582701hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604722
Supporting Variants
SamplesHG02587
Known GenesANKRD45
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061602
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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