A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709330



Internal ID21231107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154378946..154379265hg38UCSC Ensembl
chr3:154096735..154097054hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807961
Supporting Variants
Samples
Known GenesGPR149
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709330
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.921875


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