A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064933



Internal ID19154152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56081095..56093448hg38UCSC Ensembl
Innerchr17:54158456..54170809hg19UCSC Ensembl
Innerchr17:51513455..51525808hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3812354
hg1912354
hg1812354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3267n100
Supporting Variantsnssv3566123, nssv3566122, nssv3566124
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)nsv1064933
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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