A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023319



Internal ID19112536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161396671..161439604hg38UCSC Ensembl
Innerchr6:161817703..161860636hg19UCSC Ensembl
Innerchr6:161737693..161780626hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3842934
hg1942934
hg1842934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6168n100
Supporting Variantsnssv3654527, nssv3654526
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)nsv1023319
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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