A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603101



Internal ID20976172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94155637..94354472hg38UCSC Ensembl
chr7:93784949..93983784hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38198836
hg19198836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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