A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060388



Internal ID19149607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:860866..1055442hg38UCSC Ensembl
Innerchr17:764106..958682hg19UCSC Ensembl
Innerchr17:710856..905432hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38194577
hg19194577
hg18194577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3079n100
Supporting Variantsnssv3560058
Samples
Known GenesABR, MIR3183, NXN, TIMM22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060388
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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