A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030744



Internal ID19119963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5327779..5457989hg38UCSC Ensembl
Innerchr6:5328012..5458222hg19UCSC Ensembl
Innerchr6:5273011..5403221hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38130211
hg19130211
hg18130211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747909
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)nsv1030744
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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