A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3637



Internal ID15201580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:41256648..41300887hg38UCSC Ensembl
Outerchr22:41652652..41696891hg19UCSC Ensembl
Outerchr22:39982598..40026837hg18UCSC Ensembl
Outerchr22:39977152..40021391hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3844240
hg1944240
hg1844240
hg1744240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2375
SamplesNA18555
Known GenesRANGAP1
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)nsv3637
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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