A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560338



Internal ID18858619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9026594..9052968hg38UCSC Ensembl
Innerchr17:8929911..8956285hg19UCSC Ensembl
Innerchr17:8870636..8897010hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3826375
hg1926375
hg1826375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056444
Supporting Variants
Samples
Known GenesNTN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560338
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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