A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034495



Internal ID18777029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162404070..162546064hg38UCSC Ensembl
Innerchr6:162825102..162967096hg19UCSC Ensembl
Innerchr6:162745092..162887086hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38141995
hg19141995
hg18141995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6187n100
Supporting Variantsnssv3654613
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)nsv1034495
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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