A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243444



Internal ID21304153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18463896..18509244hg38UCSC Ensembl
Outerchr17:18462631..18523147hg38UCSC Ensembl
Innerchr17:18367210..18412558hg19UCSC Ensembl
Outerchr17:18365945..18426461hg19UCSC Ensembl
Innerchr17:18307935..18353283hg18UCSC Ensembl
Outerchr17:18306670..18367186hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3860517
hg1960517
hg1860517
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169646
Supporting Variants
SamplesNGO_10
Known GenesLGALS9C, USP32P2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243444
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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