A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6726



Internal ID15537137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:53749368..53757048hg38UCSC Ensembl
Outerchr17:51826729..51834409hg19UCSC Ensembl
Outerchr17:49181728..49189408hg18UCSC Ensembl
Outerchr17:49181728..49189408hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg387681
hg197681
hg187681
hg177681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2093
Supporting Variants
SamplesNA12156
Known GenesMIR548AJ2
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)nssv6726
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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