A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604573



Internal ID20977644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23741302..23743250hg38UCSC Ensembl
chr7:23780921..23782869hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381949
hg191949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154940
Samples
Known GenesSTK31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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