A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004572



Internal ID21913915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140460342..140460440hg38UCSC Ensembl
chr7:140160142..140160240hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562359
Samples
Known GenesMKRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004572
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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