A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031827



Internal ID19121049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128097557..128176736hg38UCSC Ensembl
Innerchr6:128418702..128497881hg19UCSC Ensembl
Innerchr6:128460395..128539574hg18UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3879180
hg1979180
hg1879180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654387
Samples
Known GenesPTPRK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031827
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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