A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610948



Internal ID20984019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99837134..100086836hg38UCSC Ensembl
chr6:100285010..100534712hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38249703
hg19249703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147660
Samples
Known GenesMCHR2, MCHR2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer