A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110852



Internal ID18924099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:95197556..97700666hg38UCSC Ensembl
Outerchr10:96957313..99460423hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382503111
hg192503111
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961262
SamplesKWS1
Known GenesALDH18A1, ANKRD2, ARHGAP19, ARHGAP19-SLIT1, AVPI1, BLNK, C10orf12, C10orf129, C10orf131, C10orf62, CC2D2B, CCNJ, DNTT, ENTPD1, ENTPD1-AS1, EXOSC1, FRAT1, FRAT2, HOGA1, LCOR, LOC100505540, MIR3157, MIR5692C2, MMS19, MORN4, OPALIN, PDLIM1, PGAM1, PI4K2A, PIK3AP1, RRP12, SLIT1, SORBS1, TCTN3, TLL2, TM9SF3, UBTD1, ZDHHC16, ZNF518A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110852
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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