A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027671



Internal ID21937014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4993717..4994024hg38UCSC Ensembl
chr17:4897012..4897319hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626820
Samples
Known GenesINCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027671
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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