A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762009



Internal ID22096512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183017581..183017581hg38UCSC Ensembl
chr3:182735369..182735369hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440375
Supporting Variants
Samples
Known GenesMCCC1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762009
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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