A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065299



Internal ID19154518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19594577..19635122hg38UCSC Ensembl
Innerchr17:19497890..19538435hg19UCSC Ensembl
Innerchr17:19438482..19479027hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3840546
hg1940546
hg1840546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3560567, nssv3560578, nssv3560583, nssv3560568, nssv3560572, nssv3560563, nssv3560561, nssv3560579, nssv3560571, nssv3560565, nssv3560557, nssv3560576, nssv3560584, nssv3560566, nssv3560569, nssv3560574, nssv3560577, nssv3560580, nssv3560564, nssv3560559, nssv3560575, nssv3560570, nssv3560582, nssv3560560, nssv3560562, nssv3560573, nssv3560558, nssv3560581
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)nsv1065299
Frequency
Sample Size11257
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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