A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606323



Internal ID20979394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21710038..21710569hg38UCSC Ensembl
chr7:21749656..21750187hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156988
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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