A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181456



Internal ID21320252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14912807..14912981hg38UCSC Ensembl
chr10:14954806..14954980hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954166
Supporting Variants
SamplesHG002
Known GenesDCLRE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181456
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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