A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017506



Internal ID19106723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5443305..5550892hg38UCSC Ensembl
Innerchr6:5443538..5551125hg19UCSC Ensembl
Innerchr6:5388537..5496124hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38107588
hg19107588
hg18107588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747910
Samples
Known GenesFARS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017506
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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