A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4767



Internal ID15543193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:93671735..93683652hg38UCSC Ensembl
Outerchr4:94592886..94604803hg19UCSC Ensembl
Outerchr4:94811909..94823826hg18UCSC Ensembl
Outerchr4:94950064..94961981hg17UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3811918
hg1911918
hg1811918
hg1711918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4433
Supporting Variants
SamplesNA19129
Known GenesGRID2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv4767
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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