A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9849



Internal ID15193232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2567689..2595228hg38UCSC Ensembl
Outerchr1:2499128..2526667hg19UCSC Ensembl
Outerchr1:2480108..2516527hg18UCSC Ensembl
Outerchr1:2522410..2558829hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3827540
hg1927540
hg1836420
hg1736420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7171
Supporting Variants
SamplesNA18507
Known GenesFAM213B, LOC100133445, MMEL1, TNFRSF14
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)nssv9849
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