A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503593



Internal ID22561534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87397738..87425639hg38UCSC Ensembl
chr7:87027054..87054955hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3827902
hg1927902
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850017
Supporting Variants
Samples
Known GenesABCB4, CROT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503593
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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