A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834



Internal ID15550683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91380203..91423508hg38UCSC Ensembl
Outerchr7:91009518..91052823hg19UCSC Ensembl
Outerchr7:90847454..90890759hg18UCSC Ensembl
Outerchr7:90654169..90697474hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3843306
hg1943306
hg1843306
hg1743306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11151, nssv2670
SamplesNA15510, NA18555
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)nsv5834
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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