A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131528



Internal ID21469057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121679077..121679077hg38UCSC Ensembl
chr4:122600232..122600232hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612173
Supporting Variants
SamplesHG03125
Known GenesANXA5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131528
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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