A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv57n100



Internal ID19010425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16583102..16643671hg38UCSC Ensembl
chr1:16909597..16970166hg19UCSC Ensembl
chr1:16782184..16842753hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3860570
hg1960570
hg1860570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006221, nsv1014127
Samples
Known GenesCROCCP2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv57n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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