A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191931



Internal ID21330796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36688488..36688488hg38UCSC Ensembl
chr1:37154089..37154089hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938960
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191931
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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