A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9949



Internal ID15193353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16648908..16730542hg38UCSC Ensembl
Outerchr1:16975403..17057037hg19UCSC Ensembl
Outerchr1:16847990..16929624hg18UCSC Ensembl
Outerchr1:16720709..16802343hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3881635
hg1981635
hg1881635
hg1781635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18507
Known GenesESPNP, LOC729574, MIR3675, MST1P2
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)nssv9949
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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