A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926857



Internal ID22702085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131495988..131496702hg38UCSC Ensembl
chr7:131180747..131181461hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443620
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926857
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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