A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708221



Internal ID21230011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159816141..159816141hg38UCSC Ensembl
chr6:160237173..160237173hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813771
Supporting Variants
Samples
Known GenesPNLDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708221
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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