A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477703



Internal ID22535604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2601592..2607760hg38UCSC Ensembl
chr16:2651593..2657761hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386169
hg196169
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873149
Supporting Variants
Samples
Known GenesLOC652276, PDPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477703
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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