A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002700



Internal ID21912043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94068968..94069037hg38UCSC Ensembl
chr5:93404673..93404742hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555125
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002700
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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