A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170109



Internal ID21314170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6057529..6059063hg38UCSC Ensembl
Outerchr17:6055381..6060639hg38UCSC Ensembl
Innerchr17:5960849..5962383hg19UCSC Ensembl
Outerchr17:5958701..5963959hg19UCSC Ensembl
Innerchr17:5901573..5903107hg18UCSC Ensembl
Outerchr17:5899425..5904683hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg385259
hg195259
hg185259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245712
SamplesNGO_34
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170109
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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