A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179078



Internal ID21317874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203373207..203373266hg38UCSC Ensembl
chr1:203342335..203342394hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953964
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179078
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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