A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148800



Internal ID21466227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41719014..41719772hg38UCSC Ensembl
chr7:41758612..41759370hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578627
Supporting Variants
SamplesHG03065
Known GenesINHBA-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148800
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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