A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1007633



Internal ID16301589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135788675..136007297hg38UCSC Ensembl
Innerchr4:136709830..136928452hg19UCSC Ensembl
Innerchr4:136929280..137147902hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38218623
hg19218623
hg18218623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595517
Supporting Variants
Samples
Known GenesLINC00613
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1007633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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