A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104364



Internal ID22013598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48524248..48524382hg38UCSC Ensembl
chrX:48382636..48382770hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642096
Samples
Known GenesEBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104364
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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