A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034561



Internal ID19123783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26429034..26466954hg38UCSC Ensembl
Innerchr6:26429262..26467182hg19UCSC Ensembl
Innerchr6:26537241..26575161hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3837921
hg1937921
hg1837921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5928n100
Supporting Variantsnssv3749054, nssv3654855, nssv3654856
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)nsv1034561
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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