A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573336



Internal ID21521739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38610304..38610367hg38UCSC Ensembl
chr7:38649904..38649967hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151944
SamplesNA19238
Known GenesAMPH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573336
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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