A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063537



Internal ID19152756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9026594..9059170hg38UCSC Ensembl
Innerchr17:8929911..8962487hg19UCSC Ensembl
Innerchr17:8870636..8903212hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3832577
hg1932577
hg1832577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3097n100
Supporting Variantsnssv3560339
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)nsv1063537
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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