A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101957



Internal ID22011190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128773995..128774086hg38UCSC Ensembl
chrX:127907973..127908064hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101957
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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