A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045239



Internal ID18787770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69417465..69453026hg38UCSC Ensembl
Innerchr9:72032381..72067942hg19UCSC Ensembl
Innerchr9:71222201..71257762hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3835562
hg1935562
hg1835562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7670n100
Supporting Variantsnssv3696243
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)nsv1045239
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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