A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511706



Internal ID18809987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55247422..56219986hg38UCSC Ensembl
Innerchr10:57007182..57979747hg19UCSC Ensembl
Innerchr10:56677188..57649753hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38972565
hg19972566
hg18972566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040047
Supporting Variants
Samples
Known GenesMTRNR2L5, RNU6-59P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511706
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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