A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067013



Internal ID19156232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78610659..78622614hg38UCSC Ensembl
Innerchr17:76606741..76618696hg19UCSC Ensembl
Innerchr17:74118336..74130291hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811956
hg1911956
hg1811956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567825
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)nsv1067013
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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