A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560072



Internal ID18511667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2319186..2343258hg38UCSC Ensembl
Innerchr17:2222480..2246552hg19UCSC Ensembl
Innerchr17:2169230..2193302hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3824073
hg1924073
hg1824073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067416
Supporting Variants
Samples
Known GenesSGSM2, SNORD91A, SNORD91B, SRR, TSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560072
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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