A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv115n100



Internal ID20151731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16876990..16935740hg38UCSC Ensembl
chr1:17203485..17262235hg19UCSC Ensembl
chr1:17076072..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3858751
hg1958751
hg1858751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011009, nsv1008910, nsv1005607, nsv1001379, nsv999057, nsv1001034, nsv999431, nsv1010636, nsv1002932, nsv1013372, nsv999493, nsv1002908, nsv1013913, nsv1011835, nsv1006216, nsv1002717
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)dgv115n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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