A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5708



Internal ID15550544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:39774731..39815936hg38UCSC Ensembl
Outerchr7:39814330..39855535hg19UCSC Ensembl
Outerchr7:39780855..39822060hg18UCSC Ensembl
Outerchr7:39587570..39628775hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3841206
hg1941206
hg1841206
hg1741206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521
SamplesNA12878
Known GenesLINC00265
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)nsv5708
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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