A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447801



Internal ID22113979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40046522..40046582hg38UCSC Ensembl
chrX:39905775..39905835hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758862
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447801
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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