A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv835



Internal ID15198079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16581419..16613102hg38UCSC Ensembl
Outerchr1:16907914..16939597hg19UCSC Ensembl
Outerchr1:16780501..16812184hg18UCSC Ensembl
Outerchr1:16653220..16684903hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3831684
hg1931684
hg1831684
hg1731684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3743
Supporting Variants
SamplesNA19240
Known GenesNBPF1
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)nssv835
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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