A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029357



Internal ID18771888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26432587..26464561hg38UCSC Ensembl
Innerchr6:26432815..26464789hg19UCSC Ensembl
Innerchr6:26540794..26572768hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3831975
hg1931975
hg1831975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5927n100
Supporting Variantsnssv3654857
Samples
Known GenesBTN2A1, BTN3A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029357
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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