A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073792



Internal ID19318933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112145243..112145744hg38UCSC Ensembl
chr4:113066399..113066900hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769095
SamplesKWP1
Known GenesC4orf32
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073792
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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