A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022342



Internal ID18764876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167323382..167367706hg38UCSC Ensembl
Innerchr6:167736870..167781194hg19UCSC Ensembl
Innerchr6:167656860..167701184hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3844325
hg1944325
hg1844325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655442
Samples
Known GenesTTLL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022342
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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