A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017888



Internal ID19107105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49170488..49212891hg38UCSC Ensembl
Innerchr6:49138124..49180527hg19UCSC Ensembl
Innerchr6:49246083..49288486hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3842404
hg1942404
hg1842404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657449
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)nsv1017888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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