A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737785



Internal ID20513748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107976817..107976911hg38UCSC Ensembl
chr7:107617262..107617356hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287901
Samples
Known GenesLAMB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737785
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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