A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597901



Internal ID16038624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42629012..42630866hg38UCSC Ensembl
Innerchr5:42629114..42630968hg19UCSC Ensembl
Innerchr5:42664871..42666725hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381855
hg191855
hg181855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9734n54
Supporting Variantsnssv1029339, nssv1029338
Samples
Known GenesGHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597901
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