A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847



Internal ID15550697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93690773..93726930hg38UCSC Ensembl
Outerchr7:93320085..93356242hg19UCSC Ensembl
Outerchr7:93158021..93194178hg18UCSC Ensembl
Outerchr7:92964736..93000893hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3836158
hg1936158
hg1836158
hg1736158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5003, nssv654
SamplesNA19240, NA19129
Known GenesMIR4652
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)nsv5847
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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