A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478287



Internal ID22536188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30308435..30314238hg38UCSC Ensembl
chr16:30319756..30325559hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385804
hg195804
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872289
Supporting Variants
Samples
Known GenesLOC595101
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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