A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1006135



Internal ID16300091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121366045..121368708hg38UCSC Ensembl
Innerchr4:122287200..122289863hg19UCSC Ensembl
Innerchr4:122506650..122509313hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg382664
hg192664
hg182664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595355
Supporting Variants
Samples
Known GenesQRFPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1006135
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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