A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470247



Internal ID22528137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99548352..99555607hg38UCSC Ensembl
chr14:100014689..100021944hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387256
hg197256
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850214
Supporting Variants
Samples
Known GenesCCDC85C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470247
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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