A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000835



Internal ID21910178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37495579..37495902hg38UCSC Ensembl
chr6:37463355..37463678hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565868
Samples
Known GenesCCDC167
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000835
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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