A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034814



Internal ID18777347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162399454..162587484hg38UCSC Ensembl
Innerchr6:162820486..163008516hg19UCSC Ensembl
Innerchr6:162740476..162928506hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38188031
hg19188031
hg18188031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749599
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034814
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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