A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv170n100



Internal ID20151786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61970948..61992040hg38UCSC Ensembl
chr1:62436620..62457712hg19UCSC Ensembl
chr1:62209208..62230300hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3821093
hg1921093
hg1821093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009926, nsv1003774, nsv1011197
Samples
Known GenesINADL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv170n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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