A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058288



Internal ID19147507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19596411..19639849hg38UCSC Ensembl
Innerchr17:19499724..19543162hg19UCSC Ensembl
Innerchr17:19440316..19483754hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3843439
hg1943439
hg1843439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3560880, nssv3560882, nssv3720014, nssv3720010, nssv3720012, nssv3560879, nssv3720013, nssv3720011, nssv3560883, nssv3560881
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)nsv1058288
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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