A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447881



Internal ID22114059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73836551..73836629hg38UCSC Ensembl
chr7:73250881..73250959hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765927
Samples
Known GenesWBSCR27
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447881
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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