A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984



Internal ID15538711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24826144..24870137hg38UCSC Ensembl
Outerchr1:25152635..25196628hg19UCSC Ensembl
Outerchr1:25025222..25069215hg18UCSC Ensembl
Outerchr1:24897941..24941934hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3843994
hg1943994
hg1843994
hg1743994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7076
Supporting Variants
SamplesNA12878
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)nssv3984
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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