A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060644



Internal ID19149863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79349606..79385150hg38UCSC Ensembl
Innerchr17:77345688..77381232hg19UCSC Ensembl
Innerchr17:74857283..74892827hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3835545
hg1935545
hg1835545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567836
Samples
Known GenesRBFOX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060644
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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