A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061229



Internal ID19150448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36779662..36790071hg38UCSC Ensembl
Innerchr17:35136847..35147345hg19UCSC Ensembl
Innerchr17:32210960..32221458hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810410
hg1910499
hg1810499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562541
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)nsv1061229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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