A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001511



Internal ID18845871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:94386257..97001907hg38UCSC Ensembl
Outerchr9:97148539..99764189hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382615651
hg192615651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147999
Supporting Variants
SamplesKWB1
Known GenesAAED1, C9orf3, CDC14B, ERCC6L2, FANCC, FBP1, FBP2, HABP4, HIATL1, HIATL2, HSD17B3, LINC00092, LINC00476, LOC100132781, LOC100507346, LOC158434, LOC158435, LOC441454, LOC441455, MIR2278, MIR23B, MIR24-1, MIR27B, MIR3074, MIR6081, NUTM2G, PTCH1, SLC35D2, ZNF367, ZNF510, ZNF782
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001511
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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