A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427309



Internal ID22485179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39557433..39558156hg38UCSC Ensembl
chr4:39559053..39559776hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892563
Supporting Variants
Samples
Known GenesMIR1273H, SMIM14, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427309
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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