A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616956



Internal ID20990027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35345808..35354998hg38UCSC Ensembl
chr7:35385418..35394608hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg389191
hg199191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153681
Samples
Known GenesLOC401324
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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