A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677237



Internal ID21199088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50563849..50563908hg38UCSC Ensembl
chr16:50597760..50597819hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795180
Supporting Variants
Samples
Known GenesNKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677237
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.133333


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