A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615593



Internal ID21563898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46683678..46683678hg38UCSC Ensembl
chrX:46543113..46543113hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167577
SamplesNA18534
Known GenesSLC9A7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615593
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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