A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041584



Internal ID19130803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37545448..37605332hg38UCSC Ensembl
Innerchr10:37834376..37894260hg19UCSC Ensembl
Innerchr10:37874382..37934266hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3859885
hg1959885
hg1859885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707756
Samples
Known GenesMTRNR2L7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041584
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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