A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123438



Internal ID18919056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:232613188..232613253hg38UCSC Ensembl
Outerchr2:233477898..233477963hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973198
SamplesKWS2
Known GenesEFHD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123438
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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