A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4190n100



Internal ID19014558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234032646..234055672hg38UCSC Ensembl
chr2:234941290..234964316hg19UCSC Ensembl
chr2:234606029..234629055hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3823027
hg1923027
hg1823027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006053, nsv1007335, nsv1001846
Samples
Known GenesSPP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4190n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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