A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615585



Internal ID20988656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20149029..20203615hg38UCSC Ensembl
chr7:20188652..20243238hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3854587
hg1954587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156869
Samples
Known GenesMACC1, MACC1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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