A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9691



Internal ID15193426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16676324..16766237hg38UCSC Ensembl
Outerchr1:17002819..17092732hg19UCSC Ensembl
Outerchr1:16875406..16965319hg18UCSC Ensembl
Outerchr1:16748125..16838038hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3889914
hg1989914
hg1889914
hg1789914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18507
Known GenesESPNP, LOC729574, MIR3675, 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)nssv9691
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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