A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696521



Internal ID18648116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138076863..138098496hg38UCSC Ensembl
Innerchr9:140971315..140992948hg19UCSC Ensembl
Innerchr9:140091136..140112769hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3821634
hg1921634
hg1821634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036517
Supporting Variants
Samples
Known GenesCACNA1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696521
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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