A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562857



Internal ID21887212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40609853..40609913hg38UCSC Ensembl
chr7:40649452..40649512hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002725
Supporting Variants
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562857
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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