A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007797



Internal ID21917140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140477600..140477735hg38UCSC Ensembl
chr7:140177400..140177535hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577202
Samples
Known GenesMKRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007797
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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