A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516923



Internal ID15444216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5455252..5456919hg38UCSC Ensembl
Innerchr19:5455263..5456930hg19UCSC Ensembl
Innerchr19:5406263..5407930hg18UCSC Ensembl
Innerchr19:5406263..5407930hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381668
hg191668
hg181668
hg171668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672662, nssv655000, nssv691873, nssv658229, nssv675765, nssv702892
Samples
Known GenesZNRF4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516923
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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