A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023581



Internal ID18766114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26432587..26465156hg38UCSC Ensembl
Innerchr6:26432815..26465384hg19UCSC Ensembl
Innerchr6:26540794..26573363hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3832570
hg1932570
hg1832570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5928n100
Supporting Variantsnssv3654858
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)nsv1023581
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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