A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916



Internal ID15550773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:117185167..117230516hg38UCSC Ensembl
Outerchr7:116825221..116870570hg19UCSC Ensembl
Outerchr7:116612457..116657806hg18UCSC Ensembl
Outerchr7:116419172..116464521hg17UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3845350
hg1945350
hg1845350
hg1745350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6164
SamplesNA12156
Known GenesST7, ST7-OT3
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)nsv5916
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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