A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035823



Internal ID18778354
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 StatusM
Merged Variantsdgv7665n100
Supporting Variantsnssv3696219
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)nsv1035823
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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