A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3232n100



Internal ID22789319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46168702..46358076hg38UCSC Ensembl
chr17:44246068..44435442hg19UCSC Ensembl
chr17:41601845..41791184hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38189375
hg19189375
hg18189340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062822, nsv1059247, nsv1064565, nsv1064242, nsv1063573, nsv1058991, nsv1059170, nsv1061946, nsv1057331, nsv1060792, nsv1060357
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3232n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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