A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9572



Internal ID15539742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:89158726..89198441hg38UCSC Ensembl
Outerchr2:89458210..89497929hg19UCSC Ensembl
Outerchr2:89239325..89279044hg18UCSC Ensembl
Outerchr2:89297472..89337191hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3839716
hg1939720
hg1839720
hg1739720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2824
Supporting Variants
SamplesNA18507
Known Genes
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)nssv9572
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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