A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120052



Internal ID18910573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82270324..84067426hg38UCSC Ensembl
Outerchr15:82562665..84736178hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381797103
hg192173514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960794
SamplesKWS1
Known GenesADAMTS7P1, ADAMTSL3, AP3B2, BNC1, BTBD1, C15orf40, CPEB1, CSPG4P8, FAM103A1, FAM154B, FSD2, GOLGA6L10, GOLGA6L20, GOLGA6L9, HDGFRP3, HOMER2, LOC283692, LOC283693, LOC338963, LOC727751, LOC80154, MIR4515, RPS17, RPS17L, SCARNA15, SH3GL3, TM6SF1, UBE2Q2P2, UBE2Q2P3, WHAMM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120052
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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