A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3177n100



Internal ID22789264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45668910..45699947hg38UCSC Ensembl
chr17:43746276..43777313hg19UCSC Ensembl
chr17:41102059..41133096hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3831038
hg1931038
hg1831038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056484, nsv1064736
Samples
Known GenesCRHR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3177n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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