A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528187



Internal ID15455480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:37329795..37335181hg38UCSC Ensembl
Innerchr4:37331417..37336803hg19UCSC Ensembl
Innerchr4:37007812..37013198hg18UCSC Ensembl
Innerchr4:37153983..37159369hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg385387
hg195387
hg185387
hg175387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704743
Samples
Known GenesKIAA1239
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528187
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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