A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136824



Internal ID19256836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:22431268..22431329hg38UCSC Ensembl
Outerchr4:22432891..22432952hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956693, nssv3991839
SamplesKWS2, KWS1
Known GenesGPR125
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136824
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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