A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4676



Internal ID15196446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:173307026..173331476hg38UCSC Ensembl
Outerchr4:174228177..174252627hg19UCSC Ensembl
Outerchr4:174464752..174489202hg18UCSC Ensembl
Outerchr4:174602907..174627357hg17UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3824451
hg1924451
hg1824451
hg1724451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4610
Supporting Variants
SamplesNA19129
Known GenesGALNT7, HMGB2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv4676
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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