A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007014



Internal ID21916357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20170675..20171227hg38UCSC Ensembl
chr7:20210298..20210850hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575911
Samples
Known GenesMACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007014
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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