A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737177



Internal ID20513135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77509264..77509357hg38UCSC Ensembl
chr7:77138581..77138674hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274460
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737177
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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