A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv59n100



Internal ID19010427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16583102..16695774hg38UCSC Ensembl
chr1:16909597..17022269hg19UCSC Ensembl
chr1:16782184..16894856hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38112673
hg19112673
hg18112673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001891, nsv1011340, nsv1006458, nsv1006137, nsv1008114
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)dgv59n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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