A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918577



Internal ID22693798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21489894..21508569hg38UCSC Ensembl
chr7:21529512..21548187hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3818676
hg1918676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441908
Samples
Known GenesSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918577
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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