A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7076



Internal ID15552049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24789827..24870137hg38UCSC Ensembl
Outerchr1:25116318..25196628hg19UCSC Ensembl
Outerchr1:24988905..25069215hg18UCSC Ensembl
Outerchr1:24861624..24941934hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3880311
hg1980311
hg1880311
hg1780311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973, nssv3984, nssv1983
SamplesNA12878, NA18555, NA19240
Known GenesCLIC4
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)nsv7076
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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