A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1511



Internal ID15197503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:85497488..85536299hg38UCSC Ensembl
Outerchr2:85724611..85763422hg19UCSC Ensembl
Outerchr2:85578122..85616933hg18UCSC Ensembl
Outerchr2:85636269..85675080hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3838812
hg1938812
hg1838812
hg1738812
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7315
Supporting Variants
SamplesNA19240
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)nssv1511
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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