A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286278



Internal ID20495496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44992608..44992608hg38UCSC Ensembl
chr7:45032207..45032207hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286278
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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