A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10187



Internal ID15195925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38773155..38829981hg38UCSC Ensembl
Outerchr19:39263795..39320621hg19UCSC Ensembl
Outerchr19:43955635..44012461hg18UCSC Ensembl
Outerchr19:43955635..44012461hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3856827
hg1956827
hg1856827
hg1756827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7307
Supporting Variants
SamplesNA18956
Known GenesECH1, LGALS4, LGALS7, 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)nssv10187
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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