A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050574



Internal ID19139793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122380682..122437149hg38UCSC Ensembl
Innerchr10:124140198..124196665hg19UCSC Ensembl
Innerchr10:124130188..124186655hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3856468
hg1956468
hg1856468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv987n100
Supporting Variantsnssv3521039
Samples
Known GenesMIR3941, PLEKHA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050574
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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