A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1910



Internal ID15194507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16681981..16765078hg38UCSC Ensembl
Outerchr1:17008476..17091573hg19UCSC Ensembl
Outerchr1:16881063..16964160hg18UCSC Ensembl
Outerchr1:16753782..16836879hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3883098
hg1983098
hg1883098
hg1783098
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18555
Known GenesESPNP, LOC729574, MST1L
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)nssv1910
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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