A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9333



Internal ID15193598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8270756..8294862hg38UCSC Ensembl
Outerchr19:8335640..8359746hg19UCSC Ensembl
Outerchr19:8241640..8265746hg18UCSC Ensembl
Outerchr19:8241640..8265746hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824107
hg1924107
hg1824107
hg1724107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2401
Supporting Variants
SamplesNA18517
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)nssv9333
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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