A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570318



Internal ID21762361
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 StatusS
Merged Variantsnsv6011435
Supporting Variants
Samples
Known GenesSRRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570318
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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