A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4755n100



Internal ID22790842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61612474..61701135hg38UCSC Ensembl
chr3:61598148..61686809hg19UCSC Ensembl
chr3:61573188..61661849hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3888662
hg1988662
hg1888662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000158, nsv1001611
Samples
Known GenesPTPRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4755n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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