A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851977



Internal ID22626912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87439745..87463996hg38UCSC Ensembl
chr7:87069061..87093312hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3824252
hg1924252
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503594
Samples
Known GenesABCB4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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