A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752471



Internal ID20528331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87380346..87380346hg38UCSC Ensembl
chr7:87009662..87009662hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262015
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752471
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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