A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058055



Internal ID19147274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79191761..79238589hg38UCSC Ensembl
Innerchr17:77187843..77234671hg19UCSC Ensembl
Innerchr17:74699438..74746266hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3846829
hg1946829
hg1846829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3287n100
Supporting Variantsnssv3567832
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)nsv1058055
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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