A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033146



Internal ID18775680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31385552..31483699hg38UCSC Ensembl
Innerchr6:31353329..31451476hg19UCSC Ensembl
Innerchr6:31461308..31559455hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3898148
hg1998148
hg1898148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5942n100
Supporting Variantsnssv3655786, nssv3655787, nssv3745364, nssv3655788
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033146
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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