A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035921



Internal ID19125140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125702804..125753007hg38UCSC Ensembl
Innerchr11:125572699..125622902hg19UCSC Ensembl
Innerchr11:125077909..125128112hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3850204
hg1950204
hg1850204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503164
Samples
Known GenesPATE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035921
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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