A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447985



Internal ID22114163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:82737619..82737738hg38UCSC Ensembl
chrX:81993068..81993187hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759759
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447985
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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