A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149714



Internal ID21488932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71329041..71329041hg38UCSC Ensembl
chr6:72038744..72038744hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635001
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149714
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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