A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203976



Internal ID21342780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131654722..131654722hg38UCSC Ensembl
chr7:131339481..131339481hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927828
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203976
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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