A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126913



Internal ID18907025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91423618..91424018hg38UCSC Ensembl
Outerchr9:94185900..94186300hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4098n106
Supporting Variantsnssv3985191
SamplesKWS1
Known GenesNFIL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126913
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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