A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033419



Internal ID19122641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85764650..85840312hg38UCSC Ensembl
Innerchr6:86474368..86550030hg19UCSC Ensembl
Innerchr6:86531087..86606749hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3875663
hg1975663
hg1875663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6079n100
Supporting Variantsnssv3648898, nssv3648900, nssv3648901, nssv3648899
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033419
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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