A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177408



Internal ID21316204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151599282..151599522hg38UCSC Ensembl
chr1:151571758..151571998hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937282
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177408
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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