A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929849



Internal ID22705108
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 StatusM
Merged Variants
Supporting Variantsnssv17389311
Samples
Known GenesGCHFR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929849
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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