A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109898



Internal ID19252118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:92122238..92124872hg38UCSC Ensembl
Outerchr7:91751552..91754186hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg382635
hg192635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958314
SamplesKWS1
Known GenesCYP51A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109898
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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