A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050289



Internal ID19139508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3395247..3591499hg38UCSC Ensembl
Innerchr11:3416477..3612729hg19UCSC Ensembl
Innerchr11:3373053..3569305hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38196253
hg19196253
hg18196253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1018n100
Supporting Variantsnssv3519967
Samples
Known GenesLOC650368
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050289
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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