A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964



Internal ID15204140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:137914705..137931554hg38UCSC Ensembl
Outerchr7:137599451..137616300hg19UCSC Ensembl
Outerchr7:137249991..137266840hg18UCSC Ensembl
Outerchr7:137056706..137073555hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3816850
hg1916850
hg1816850
hg1716850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8435
SamplesNA12156
Known GenesCREB3L2
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)nsv5964
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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