A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532576



Internal ID21856932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2764604..2764604hg38UCSC Ensembl
chr1:2688412..2688412hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050166
Supporting Variants
Samples
Known GenesTTC34
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532576
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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