A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7524



Internal ID15536340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88818069..88857249hg38UCSC Ensembl
Outerchr2:89117583..89156762hg19UCSC Ensembl
Outerchr2:88898698..88937877hg18UCSC Ensembl
Outerchr2:88956845..88996024hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3839181
hg1939180
hg1839180
hg1739180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2824
Supporting Variants
SamplesNA12156
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)nssv7524
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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