A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061142



Internal ID21491814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15063769..15063823hg38UCSC Ensembl
chr1:15390265..15390319hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565031
Supporting Variants
SamplesNA19238
Known GenesKAZN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061142
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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