A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503487



Internal ID22561428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81743101..81745275hg38UCSC Ensembl
chr7:81372417..81374591hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865830
Supporting Variants
Samples
Known GenesHGF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503487
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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