A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074672



Internal ID19322798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2934272..2934773hg38UCSC Ensembl
chr4:2935999..2936500hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771447
SamplesKWP1
Known GenesMFSD10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074672
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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