A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066149



Internal ID19155368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:977083..1047718hg38UCSC Ensembl
Innerchr17:880323..950958hg19UCSC Ensembl
Innerchr17:827073..897708hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3870636
hg1970636
hg1870636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560064
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)nsv1066149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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