A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574131



Internal ID16361540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:949100..949686hg38UCSC Ensembl
Innerchr17:852340..852926hg19UCSC Ensembl
Innerchr17:799090..799676hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38587
hg19587
hg18587
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866193, nssv866187, nssv866197, nssv866191, nssv866189, nssv866196, nssv866188, nssv866194, nssv866190, nssv866192, nssv866198, nssv866186, nssv866195
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574131
Frequency
Sample Size17421
Observed Gain1
Observed Loss12
Observed Complex0
Frequencyn/a


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