A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048775



Internal ID19137994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3395247..3591436hg38UCSC Ensembl
Innerchr11:3416477..3612666hg19UCSC Ensembl
Innerchr11:3373053..3569242hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38196190
hg19196190
hg18196190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1018n100
Supporting Variantsnssv3518430
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)nsv1048775
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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