A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv71n100



Internal ID19010439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16627264..16686278hg38UCSC Ensembl
chr1:16953759..17012773hg19UCSC Ensembl
chr1:16826346..16885360hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3859015
hg1959015
hg1859015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009664, nsv1013865
Samples
Known GenesCROCCP2, LOC729574, MIR3675, MST1P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv71n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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