A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043075



Internal ID19132294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137333691..137361369hg38UCSC Ensembl
Innerchr9:140228143..140255821hg19UCSC Ensembl
Innerchr9:139347964..139375642hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3827679
hg1927679
hg1827679
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759863, nssv3759861, nssv3696515, nssv3696516, nssv3759858, nssv3759860, nssv3696514, nssv3759859, nssv3759862
Samples
Known GenesEXD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043075
Frequency
Sample Size11257
Observed Gain2
Observed Loss7
Observed Complex0
Frequencyn/a


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