A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021433



Internal ID18763967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162954728..163088834hg38UCSC Ensembl
Innerchr6:163375760..163509866hg19UCSC Ensembl
Innerchr6:163295750..163429856hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38134107
hg19134107
hg18134107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655390
Samples
Known GenesPACRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021433
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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