A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064752



Internal ID19153971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77754686..77802158hg38UCSC Ensembl
Innerchr17:75750768..75798240hg19UCSC Ensembl
Innerchr17:73262363..73309835hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3847473
hg1947473
hg1847473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567817, nssv3567815, nssv3567816
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)nsv1064752
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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