A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064897



Internal ID19154116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57321283..57373857hg38UCSC Ensembl
Innerchr17:55398644..55451218hg19UCSC Ensembl
Innerchr17:52753643..52806217hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3852575
hg1952575
hg1852575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567702
Samples
Known GenesMSI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064897
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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