A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079967



Internal ID21437389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9062355..9062411hg38UCSC Ensembl
chr12:9214951..9215007hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588443
Supporting Variants
SamplesHG00731
Known GenesLINC00612
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079967
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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