A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897



Internal ID15550752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:110520764..110568177hg38UCSC Ensembl
Outerchr7:110160821..110208234hg19UCSC Ensembl
Outerchr7:109948057..109995470hg18UCSC Ensembl
Outerchr7:109754772..109802185hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3847414
hg1947414
hg1847414
hg1747414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9726, nssv3566
SamplesNA18507, NA12878
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)nsv5897
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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