A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764954



Internal ID19309012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6708782..6708850hg38UCSC Ensembl
chr4:6710509..6710577hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073726
Supporting Variants
SamplesKWP1
Known GenesMRFAP1L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764954
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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