A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139852



Internal ID21442550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130079869..130079928hg38UCSC Ensembl
chr7:129719709..129719768hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580657
Supporting Variants
SamplesHG00732
Known GenesKLHDC10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139852
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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