A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446527



Internal ID22504397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:930402..2311664hg38UCSC Ensembl
chr7:970038..2351299hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381381263
hg191381262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911215
Supporting Variants
Samples
Known GenesADAP1, C7orf50, COX19, CYP2W1, ELFN1, FTSJ2, GPER1, GPR146, INTS1, MAD1L1, MAFK, MICALL2, MIR339, MIR4655, MIR6836, NUDT1, PSMG3, PSMG3-AS1, SNX8, TFAMP1, TMEM184A, UNCX, ZFAND2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446527
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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