A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426771



Internal ID21084324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60867890..60868514hg38UCSC Ensembl
chr8:61780449..61781073hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168693
Samples
Known GenesCHD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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