A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051541



Internal ID18794072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130499187..130530031hg38UCSC Ensembl
Innerchr9:133374574..133405418hg19UCSC Ensembl
Innerchr9:132364395..132395239hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3830845
hg1930845
hg1830845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695255
Samples
Known GenesASS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051541
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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