A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4100n100



Internal ID22790187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167166913..167215737hg38UCSC Ensembl
chr2:168023423..168072247hg19UCSC Ensembl
chr2:167731669..167780493hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3848825
hg1948825
hg1848825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015022, nsv1002883, nsv997489
Samples
Known GenesXIRP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4100n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer