A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4755



Internal ID15196528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:74746924..78636095hg38UCSC Ensembl
Outerchr4:75672134..79557249hg19UCSC Ensembl
Outerchr4:75891158..79776273hg18UCSC Ensembl
Outerchr4:76029313..79914428hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg383889172
hg193885116
hg183885116
hg173885116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7363
Supporting Variants
SamplesNA19129
Known GenesANXA3, ART3, BTC, C4orf26, CCDC158, CCNG2, CCNI, CDKL2, CNOT6L, CXCL10, CXCL11, CXCL13, CXCL9, FAM47E, FAM47E-STBD1, FRAS1, G3BP2, LOC441025, MIR4450, MRPL1, NAAA, NUP54, PARM1, PPEF2, RCHY1, SCARB2, SDAD1, SEPT11, SHROOM3, SOWAHB, STBD1, THAP6, USO1
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)nssv4755
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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