A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731671



Internal ID20507591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216263428..216263522hg38UCSC Ensembl
chr2:217128151..217128245hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259072
Samples
Known GenesMARCH4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731671
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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