A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144931



Internal ID21459848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130887277..130887277hg38UCSC Ensembl
chr7:130572036..130572036hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643020
Supporting Variants
SamplesHG02818
Known GenesLOC646329
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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