A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058849



Internal ID19148068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17404695..17445234hg38UCSC Ensembl
Innerchr17:17308009..17348548hg19UCSC Ensembl
Innerchr17:17248734..17289273hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3840540
hg1940540
hg1840540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3109n100
Supporting Variantsnssv3560428, nssv3719937, nssv3560429
Samples
Known GenesSMCR9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058849
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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