A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176905



Internal ID21315701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165761972..165762252hg38UCSC Ensembl
chr1:165731209..165731489hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946407
Supporting Variants
SamplesHG002
Known GenesTMCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176905
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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