A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3861



Internal ID15191902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16583163..16857087hg38UCSC Ensembl
Outerchr1:16909658..17183582hg19UCSC Ensembl
Outerchr1:16782245..17056169hg18UCSC Ensembl
Outerchr1:16654964..16928888hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38273925
hg19273925
hg18273925
hg17273925
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA12878
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)nssv3861
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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