A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696218



Internal ID18647813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68787002..69188723hg38UCSC Ensembl
Innerchr9:71401918..71803639hg19UCSC Ensembl
Innerchr9:70591738..70993459hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38401722
hg19401722
hg18401722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047540
Supporting Variants
Samples
Known GenesFXN, PIP5K1B, PRKACG, TJP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696218
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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