A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431336



Internal ID22489206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88128904..88157546hg38UCSC Ensembl
chr6:88838623..88867265hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3828643
hg1928643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907523
Supporting Variants
Samples
Known GenesCNR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431336
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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