A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv60n100



Internal ID19010428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16583102..16703738hg38UCSC Ensembl
chr1:16909597..17030233hg19UCSC Ensembl
chr1:16782184..16902820hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38120637
hg19120637
hg18120637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013734, nsv997399
Samples
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv60n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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