A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442620



Internal ID22108803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48964742..48964742hg38UCSC Ensembl
chrX:48822003..48822003hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767553
Samples
Known GenesKCND1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442620
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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