A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055849



Internal ID19145068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14494839..14521563hg38UCSC Ensembl
Innerchr17:14398156..14424880hg19UCSC Ensembl
Innerchr17:14338881..14365605hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3826725
hg1926725
hg1826725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3103n100
Supporting Variantsnssv3560374
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)nsv1055849
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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