A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526576



Internal ID15107183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155230087..155258266hg38UCSC Ensembl
Innerchr6:155551221..155579400hg19UCSC Ensembl
Innerchr6:155592913..155621092hg18UCSC Ensembl
Innerchr6:155643334..155671513hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3828180
hg1928180
hg1828180
hg1728180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702894
Samples
Known GenesTFB1M, TIAM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526576
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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