A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016398



Internal ID19105617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37180654..37335200hg38UCSC Ensembl
Innerchr9:37180651..37335197hg19UCSC Ensembl
Innerchr9:37170651..37325197hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38154547
hg19154547
hg18154547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688888
Samples
Known GenesZCCHC7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016398
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