A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044497



Internal ID18787028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119533784..119601465hg38UCSC Ensembl
Innerchr10:121293296..121360977hg19UCSC Ensembl
Innerchr10:121283286..121350967hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3867682
hg1967682
hg1867682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516193
Samples
Known GenesRGS10, TIAL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044497
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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