A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606923



Internal ID20979994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18166201..18350900hg38UCSC Ensembl
chr7:18205824..18390523hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38184700
hg19184700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6610n223
Supporting Variantsnssv18154796
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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