A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560295



Internal ID18858576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6230914hg38UCSC Ensembl
Innerchr17:6106486..6134234hg19UCSC Ensembl
Innerchr17:6047210..6074958hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3827749
hg1927749
hg1827749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057129
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)nssv3560295
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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