A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639497



Internal ID21587802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369854..74369854hg38UCSC Ensembl
chr7:73784184..73784184hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157987
SamplesHG03125
Known GenesCLIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639497
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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