A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167577



Internal ID21487262
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 StatusS
Merged Variantsnsv5615593
Supporting Variants
SamplesNA18534
Known GenesSLC9A7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167577
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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