A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696219



Internal ID18647814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68850223..69286756hg38UCSC Ensembl
Innerchr9:71465139..71901672hg19UCSC Ensembl
Innerchr9:70654959..71091492hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38436534
hg19436534
hg18436534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035823
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)nssv3696219
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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