A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055257



Internal ID19144476
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 StatusM
Merged Variants
Supporting Variantsnssv3566104
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)nsv1055257
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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