A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999174



Internal ID18812024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79291781..79591202hg38UCSC Ensembl
Innerchr4:80212935..80512356hg19UCSC Ensembl
Innerchr4:80431959..80731380hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38299422
hg19299422
hg18299422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633886, nssv3633887, nssv3633888
Samples
Known GenesGK2, LINC00989, LINC01088, NAA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999174
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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