A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703178



Internal ID15439830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143638077..143654020hg38UCSC Ensembl
Innerchr6:143959214..143975157hg19UCSC Ensembl
Innerchr6:144000907..144016850hg18UCSC Ensembl
Innerchr6:144000907..144016850hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3815944
hg1915944
hg1815944
hg1715944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517253
Supporting Variants
Samples
Known GenesPHACTR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703178
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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