A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412715



Internal ID21070268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71524731..71551179hg38UCSC Ensembl
chr5:70820558..70847006hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3826449
hg1926449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133360
Samples
Known GenesBDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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