A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv124n100



Internal ID22786211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16909177..16935740hg38UCSC Ensembl
chr1:17235672..17262235hg19UCSC Ensembl
chr1:17108259..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3826564
hg1926564
hg1826564
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008279, nsv1012684, nsv1013207, nsv1005306, nsv1005265
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv124n100
Frequency
Sample Size11257
Observed Gain22
Observed Loss28
Observed Complex0
Frequencyn/a


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