A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560888



Internal ID18859169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19596411..19640825hg38UCSC Ensembl
Innerchr17:19499724..19544138hg19UCSC Ensembl
Innerchr17:19440316..19484730hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3844415
hg1944415
hg1844415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064603
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)nssv3560888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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