A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10485



Internal ID15195627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16561870..16886061hg38UCSC Ensembl
Outerchr1:16888365..17212556hg19UCSC Ensembl
Outerchr1:16760952..17085143hg18UCSC Ensembl
Outerchr1:16633671..16957862hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38324192
hg19324192
hg18324192
hg17324192
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18956
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)nssv10485
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer