A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764581



Internal ID19313346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25030477..25031378hg38UCSC Ensembl
chr4:25032099..25033000hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073313
Supporting Variants
SamplesKWP1
Known GenesLGI2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764581
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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