A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv69n100



Internal ID19010437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16617106..16643949hg38UCSC Ensembl
chr1:16943601..16970444hg19UCSC Ensembl
chr1:16816188..16843031hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3826844
hg1926844
hg1826844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008125, nsv997712
Samples
Known GenesCROCCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv69n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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