A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026962



Internal ID18769493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68335100..68742689hg38UCSC Ensembl
Innerchr9:70950016..71357605hg19UCSC Ensembl
Innerchr9:70139836..70547425hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38407590
hg19407590
hg18407590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696216
Samples
Known GenesLOC101927015, PGM5, PGM5-AS1, PIP5K1B, TMEM252
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026962
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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