A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509047



Internal ID22566997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100126595..100134180hg38UCSC Ensembl
chr7:99724218..99731803hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg387586
hg197586
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867480
Supporting Variants
Samples
Known GenesMBLAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509047
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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