A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190896



Internal ID21329764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24634837..24634837hg38UCSC Ensembl
chr1:24961328..24961328hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925032
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190896
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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