A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072410



Internal ID15925596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125860810..125865498hg38UCSC Ensembl
Innerchr6:126181956..126186644hg19UCSC Ensembl
Innerchr6:126223649..126228337hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg384689
hg194689
hg184689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604606
Supporting Variants
Samples
Known GenesNCOA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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