A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560343



Internal ID18858624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10238301..10274862hg38UCSC Ensembl
Innerchr17:10141618..10178179hg19UCSC Ensembl
Innerchr17:10082343..10118904hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3836562
hg1936562
hg1836562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060012
Supporting Variants
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)nssv3560343
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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