A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5632n100



Internal ID20157248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36927550..37039755hg38UCSC Ensembl
chr5:36927652..37039857hg19UCSC Ensembl
chr5:36963409..37075614hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38112206
hg19112206
hg18112206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029319, nsv1029936, nsv1017947, nsv1030883, nsv1023362
Samples
Known GenesNIPBL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5632n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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