A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4128n100



Internal ID22790215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185576655..185999663hg38UCSC Ensembl
chr2:186441382..186864390hg19UCSC Ensembl
chr2:186149627..186572635hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38423009
hg19423009
hg18423009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007052, nsv1009118
Samples
Known GenesFSIP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4128n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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