A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025072



Internal ID19114290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17577143..17632545hg38UCSC Ensembl
Innerchr9:17577141..17632543hg19UCSC Ensembl
Innerchr9:17567141..17622543hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3855403
hg1955403
hg1855403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7466n100
Supporting Variantsnssv3690648
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025072
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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