A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137670



Internal ID21512603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37330789..37331362hg38UCSC Ensembl
chr4:37332411..37332984hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565710
Supporting Variants
SamplesNA24385
Known GenesKIAA1239
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137670
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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