A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10995



Internal ID15192897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38777034..38830942hg38UCSC Ensembl
Outerchr19:39267674..39321582hg19UCSC Ensembl
Outerchr19:43959514..44013422hg18UCSC Ensembl
Outerchr19:43959514..44013422hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3853909
hg1953909
hg1853909
hg1753909
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7307
Supporting Variants
SamplesNA15510
Known GenesECH1, LGALS4, LGALS7B
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)nssv10995
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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