A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053340



Internal ID18795871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132263187..132282644hg38UCSC Ensembl
Innerchr9:135138574..135158031hg19UCSC Ensembl
Innerchr9:134128395..134147852hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3819458
hg1919458
hg1819458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696402
Samples
Known GenesSETX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053340
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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