A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6178n100



Internal ID20157794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162195980..162657210hg38UCSC Ensembl
chr6:162617012..163078242hg19UCSC Ensembl
chr6:162537002..162998232hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38461231
hg19461231
hg18461231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016439, nsv1033111, nsv1020023, nsv1023671, nsv1028992
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)dgv6178n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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