A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032358



Internal ID19121580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38355969..38448079hg38UCSC Ensembl
Innerchr6:38323745..38415855hg19UCSC Ensembl
Innerchr6:38431723..38523833hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3892111
hg1992111
hg1892111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657427
Samples
Known GenesBTBD9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032358
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