A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165001



Internal ID21462567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102276707..102276707hg38UCSC Ensembl
chrX:101531665..101531665hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619597
Supporting Variants
SamplesHG03009
Known GenesNXF2, NXF2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165001
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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