A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035525



Internal ID19124744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96227010..96246624hg38UCSC Ensembl
Innerchr11:95960174..95979788hg19UCSC Ensembl
Innerchr11:95599822..95619436hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3819615
hg1919615
hg1819615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1254n100
Supporting Variantsnssv3503875
Samples
Known GenesMAML2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035525
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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