A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126644



Internal ID18939245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:23944609..23947409hg38UCSC Ensembl
Outerchr3:23986100..23988900hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984909
SamplesKWS1
Known GenesNR1D2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126644
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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