A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566104



Internal ID18864385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54541869..54679911hg38UCSC Ensembl
Innerchr17:52619230..52757272hg19UCSC Ensembl
Innerchr17:49974229..50112271hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38138043
hg19138043
hg18138043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055257
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)nssv3566104
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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