A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141403



Internal ID21470739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40048595..40049101hg38UCSC Ensembl
chr7:40088194..40088700hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582127
Supporting Variants
SamplesHG03125
Known GenesCDK13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141403
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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