A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575931



Internal ID16363340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69153832..69230502hg38UCSC Ensembl
Innerchr17:67149973..67226643hg19UCSC Ensembl
Innerchr17:64661568..64738238hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3876671
hg1976671
hg1876671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5757n54
Supporting Variantsnssv1149793
Samples1780862176_A
Known GenesABCA10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575931
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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