A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389311



Internal ID22447181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40766261..40766336hg38UCSC Ensembl
chr15:41058459..41058534hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929849
Supporting Variants
Samples
Known GenesGCHFR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389311
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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