A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503958



Internal ID22561901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137072072..137083613hg38UCSC Ensembl
chr7:136756819..136768360hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3811542
hg1911542
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862234
Supporting Variants
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503958
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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