A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031229



Internal ID19120450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26428086..26466954hg38UCSC Ensembl
Innerchr6:26428314..26467182hg19UCSC Ensembl
Innerchr6:26536293..26575161hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3838869
hg1938869
hg1838869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5928n100
Supporting Variantsnssv3749050
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)nsv1031229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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