A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5995



Internal ID15537869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:51620165..51650197hg38UCSC Ensembl
Outerchr5:50915999..50946031hg19UCSC Ensembl
Outerchr5:50951756..50981788hg18UCSC Ensembl
Outerchr5:50951756..50981788hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3830033
hg1930033
hg1830033
hg1730033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4823
Supporting Variants
SamplesNA12156
Known Genes
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)nssv5995
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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