A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601808



Internal ID20974879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16603553..16608654hg38UCSC Ensembl
chr7:16643178..16648279hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152310
Samples
Known GenesANKMY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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