A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509612



Internal ID22567562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12359017..12360057hg38UCSC Ensembl
chr7:12398643..12399683hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381041
hg191041
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845875
Supporting Variants
Samples
Known GenesVWDE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509612
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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