A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574500



Internal ID16015223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16768138..16814874hg38UCSC Ensembl
Innerchr17:16671452..16718188hg19UCSC Ensembl
Innerchr17:16612177..16658913hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3846737
hg1946737
hg1846737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5477n54
Supporting Variantsnssv868807, nssv868808
Samples
Known GenesCCDC144A, FAM106CP, USP32P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574500
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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