A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719166



Internal ID19017447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10209908..10262660hg38UCSC Ensembl
Innerchr17:10113225..10165977hg19UCSC Ensembl
Innerchr17:10053950..10106702hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3852753
hg1952753
hg1852753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060144
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3719166
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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