A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607142



Internal ID20980213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75064633..75069155hg38UCSC Ensembl
chr7:74480446..74484969hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384523
hg194524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159573
Samples
Known GenesWBSCR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607142
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