A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035641



Internal ID19124860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50135065..50614043hg38UCSC Ensembl
Innerchr11:50094236..50573214hg19UCSC Ensembl
Innerchr11:50050812..50529790hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38478979
hg19478979
hg18478979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1136n100
Supporting Variantsnssv3503989
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035641
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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