A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065322



Internal ID21434157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39784524..39784644hg38UCSC Ensembl
chr1:40250196..40250316hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574813
Supporting Variants
SamplesHG00731
Known GenesBMP8B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065322
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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