A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022177



Internal ID18764711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68394179..68532724hg38UCSC Ensembl
Innerchr9:71009095..71147640hg19UCSC Ensembl
Innerchr9:70198915..70337460hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38138546
hg19138546
hg18138546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759751
Samples
Known GenesPGM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022177
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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