A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061429



Internal ID19150648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56081671..56095450hg38UCSC Ensembl
Innerchr17:54159032..54172811hg19UCSC Ensembl
Innerchr17:51514031..51527810hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3813780
hg1913780
hg1813780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3267n100
Supporting Variantsnssv3566132, nssv3724984, nssv3566129, nssv3566131, nssv3566130
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)nsv1061429
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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