A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560349



Internal ID18511944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10622619..10784575hg38UCSC Ensembl
Innerchr17:10525936..10687892hg19UCSC Ensembl
Innerchr17:10466661..10628617hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38161957
hg19161957
hg18161957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065819
Supporting Variants
Samples
Known GenesADPRM, MAGOH2, MYH3, SCO1, TMEM220, TMEM220-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560349
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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