A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014463



Internal ID21923806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73836551..73836629hg38UCSC Ensembl
chr7:73250881..73250959hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566724
Samples
Known GenesWBSCR27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014463
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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