A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060177



Internal ID19149396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33342525..33365430hg38UCSC Ensembl
Innerchr17:31669543..31692448hg19UCSC Ensembl
Innerchr17:28693656..28716561hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3822906
hg1922906
hg1822906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561061
Samples
Known GenesASIC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060177
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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