A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015524



Internal ID18758058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17350845..17419426hg38UCSC Ensembl
Innerchr9:17350843..17419424hg19UCSC Ensembl
Innerchr9:17340843..17409424hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3868582
hg1968582
hg1868582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690647
Samples
Known GenesCNTLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015524
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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