A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572531



Internal ID21764574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37437674..37438001hg38UCSC Ensembl
chr7:37477277..37477604hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017786
Supporting Variants
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572531
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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