A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177140



Internal ID21315936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169761276..169761583hg38UCSC Ensembl
chr1:169730417..169730724hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933394
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177140
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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