A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061776



Internal ID19150995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48660164..48704615hg38UCSC Ensembl
Innerchr17:46737526..46781977hg19UCSC Ensembl
Innerchr17:44092525..44136976hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3844452
hg1944452
hg1844452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3262n100
Supporting Variantsnssv3724974
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061776
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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