A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3851



Internal ID15191892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16563034..16882048hg38UCSC Ensembl
Outerchr1:16889529..17208543hg19UCSC Ensembl
Outerchr1:16762116..17081130hg18UCSC Ensembl
Outerchr1:16634835..16953849hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38319015
hg19319015
hg18319015
hg17319015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA12878
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
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)nssv3851
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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