A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107316



Internal ID22016549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44531270..44531355hg38UCSC Ensembl
chrX:44390516..44390601hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640238
Samples
Known GenesFUNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107316
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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