A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141704



Internal ID21505714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66392249..66392633hg38UCSC Ensembl
chr7:65857236..65857620hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565642
Supporting Variants
SamplesNA19650
Known GenesLINC00174
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141704
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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