A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566212



Internal ID21758255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54545977..54545977hg38UCSC Ensembl
chr7:54613670..54613670hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063209
Supporting Variants
Samples
Known GenesVSTM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566212
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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