A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145035



Internal ID18902112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:94757749..94758449hg38UCSC Ensembl
Outerchr4:95678900..95679600hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981652
SamplesKWS1
Known GenesBMPR1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145035
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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