A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056174



Internal ID18798705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81416245..81457288hg38UCSC Ensembl
Innerchr17:79390045..79424314hg19UCSC Ensembl
Innerchr17:77004640..77038909hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3841044
hg1934270
hg1834270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567883
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056174
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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