A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025700



Internal ID19114917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:133405126..133427620hg38UCSC Ensembl
Innerchr6:133726264..133748758hg19UCSC Ensembl
Innerchr6:133767957..133790451hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3822495
hg1922495
hg1822495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6147n100
Supporting Variantsnssv3654395
Samples
Known GenesEYA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025700
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