A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033003



Internal ID19122225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26428086..26465156hg38UCSC Ensembl
Innerchr6:26428314..26465384hg19UCSC Ensembl
Innerchr6:26536293..26573363hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3837071
hg1937071
hg1837071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5928n100
Supporting Variantsnssv3654852, nssv3749049, nssv3654853
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)nsv1033003
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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