A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7441



Internal ID15189737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40094718..40107207hg38UCSC Ensembl
Outerchr19:40600625..40613114hg19UCSC Ensembl
Outerchr19:45292465..45304954hg18UCSC Ensembl
Outerchr19:45292465..45304954hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3812490
hg1912490
hg1812490
hg1712490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2488
Supporting Variants
SamplesNA12156
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)nssv7441
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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