A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094002



Internal ID21501002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75111633..75112142hg38UCSC Ensembl
chr17:73107728..73108237hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591663
Supporting Variants
SamplesNA19239
Known GenesARMC7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094002
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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