A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045274



Internal ID18787805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69417465..69434676hg38UCSC Ensembl
Innerchr9:72032381..72049592hg19UCSC Ensembl
Innerchr9:71222201..71239412hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3817212
hg1917212
hg1817212
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696233, nssv3696238, nssv3696236, nssv3696234, nssv3696235, nssv3696237, nssv3696240, nssv3696241, nssv3696239
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045274
Frequency
Sample Size29084
Observed Gain8
Observed Loss1
Observed Complex0
Frequencyn/a


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