A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1519



Internal ID15198875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:95761051..96022127hg38UCSC Ensembl
Outerchr2:96426799..96687875hg19UCSC Ensembl
Outerchr2:95790526..96051602hg18UCSC Ensembl
Outerchr2:95848673..96109749hg17UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38261077
hg19261077
hg18261077
hg17261077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7322
Supporting Variants
SamplesNA19240
Known GenesFAHD2CP, GPAT2, LINC00342
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)nssv1519
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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