A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011435



Internal ID21920778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76137185..76258784hg38UCSC Ensembl
chr7:75766503..75888102hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38121600
hg19121600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570318
Samples
Known GenesSRRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011435
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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