A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508343



Internal ID22566292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:61071231..61088604hg38UCSC Ensembl
chr7:61054332..61071329hg19UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg3817374
hg1916998
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508343
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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