A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033546



Internal ID18776079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5875201..5900427hg38UCSC Ensembl
Innerchr9:5875201..5900427hg19UCSC Ensembl
Innerchr9:5865201..5890427hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3825227
hg1925227
hg1825227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692425
Samples
Known GenesMLANA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033546
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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