A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017824



Internal ID18760357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26425182..26465156hg38UCSC Ensembl
Innerchr6:26425410..26465384hg19UCSC Ensembl
Innerchr6:26533389..26573363hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3839975
hg1939975
hg1839975
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749047, nssv3654846
Samples
Known GenesBTN2A1, BTN2A3P, BTN3A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017824
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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