A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567706



Internal ID18519301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58876760..59269333hg38UCSC Ensembl
Innerchr17:56954121..57346694hg19UCSC Ensembl
Innerchr17:54308903..54701476hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38392574
hg19392574
hg18392574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065063
Supporting Variants
Samples
Known GenesGDPD1, MIR301A, MIR454, PPM1E, PRR11, SKA2, SMG8, TRIM37
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567706
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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