A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960794



Internal ID18871395
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 StatusS
Merged Variantsnsv1120052
Supporting Variants
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)nssv3960794
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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