A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1016863



Internal ID15964133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173169007..173169855hg38UCSC Ensembl
Innerchr4:174090158..174091006hg19UCSC Ensembl
Innerchr4:174326733..174327581hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38849
hg19849
hg18849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596225
Supporting Variants
Samples
Known GenesGALNT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1016863
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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