A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157539



Internal ID21463135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156703824..156703824hg38UCSC Ensembl
chr6:157024958..157024958hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626479
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157539
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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