A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044088



Internal ID21953379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130108312..130108312hg38UCSC Ensembl
chrX:129242287..129242287hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639487
Samples
Known GenesELF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044088
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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