A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124452



Internal ID18903393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:94565686..94565740hg38UCSC Ensembl
Outerchr9:97327968..97328022hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992523, nssv3960392
SamplesKWS2, KWS1
Known GenesFBP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124452
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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