A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7920



Internal ID15535944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:6905150..6913436hg38UCSC Ensembl
Outerchr4:6906877..6915163hg19UCSC Ensembl
Outerchr4:6957778..6966064hg18UCSC Ensembl
Outerchr4:7024949..7033235hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg388287
hg198287
hg188287
hg178287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4216
Supporting Variants
SamplesNA12156
Known GenesTBC1D14
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)nssv7920
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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