A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057804



Internal ID19147023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36714218..36729840hg38UCSC Ensembl
Innerchr17:35070662..35086148hg19UCSC Ensembl
Innerchr17:32144775..32160261hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3815623
hg1915487
hg1815487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562539
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)nsv1057804
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer