A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10993



Internal ID15192895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35346502..35375933hg38UCSC Ensembl
Outerchr19:35837405..35866835hg19UCSC Ensembl
Outerchr19:40529245..40558675hg18UCSC Ensembl
Outerchr19:40529245..40558675hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3829432
hg1929431
hg1829431
hg1729431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2471
Supporting Variants
SamplesNA15510
Known GenesCD22, FFAR1, FFAR3
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)nssv10993
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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