A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1001630



Internal ID16295586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64334499..64397714hg38UCSC Ensembl
Innerchr4:65200217..65263432hg19UCSC Ensembl
Innerchr4:64882812..64946027hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3863216
hg1963216
hg1863216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594473
Supporting Variants
Samples
Known GenesTECRL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1001630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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