A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7744



Internal ID15552784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:40237065..40281451hg38UCSC Ensembl
Outerchr11:40258615..40303001hg19UCSC Ensembl
Outerchr11:40215191..40259577hg18UCSC Ensembl
Outerchr11:40215191..40259577hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3844387
hg1944387
hg1844387
hg1744387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4625
SamplesNA19129
Known GenesLRRC4C
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)nsv7744
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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