A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611187



Internal ID20984258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74381364..74386135hg38UCSC Ensembl
chr7:73795694..73800465hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384772
hg194772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159531
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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