A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562726



Internal ID16350135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92215820..92315411hg38UCSC Ensembl
Innerchr13:92868073..92967664hg19UCSC Ensembl
Innerchr13:91666074..91765665hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3899592
hg1999592
hg1899592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817477
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562726
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