A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616578



Internal ID20989649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97160091..97163548hg38UCSC Ensembl
chr7:96789403..96792860hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383458
hg193458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160782
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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