A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029936



Internal ID18772467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36927550..37025769hg38UCSC Ensembl
Innerchr5:36927652..37025871hg19UCSC Ensembl
Innerchr5:36963409..37061628hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3898220
hg1998220
hg1898220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5632n100
Supporting Variantsnssv3637078
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)nsv1029936
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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