A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026793



Internal ID18769324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57855503..58096352hg38UCSC Ensembl
Innerchr6:58181781..58422630hg19UCSC Ensembl
Innerchr6:58289740..58530589hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38240850
hg19240850
hg18240850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657541
Samples
Known GenesGUSBP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026793
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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