A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165601



Internal ID21482894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125321975..125321975hg38UCSC Ensembl
chrX:124455824..124455824hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604718
Supporting Variants
SamplesHG03732
Known GenesLOC100129520
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165601
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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