A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122110



Internal ID18913413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:71031873..71043073hg38UCSC Ensembl
Outerchr5:70327700..70338900hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3811201
hg1911201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969552
SamplesKWS2
Known GenesGTF2H2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122110
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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