A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570444



Internal ID21762487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36363390..36363390hg38UCSC Ensembl
chr6:36331167..36331167hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070120
Supporting Variants
Samples
Known GenesETV7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570444
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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