A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4610



Internal ID15202651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:173295875..173331476hg38UCSC Ensembl
Outerchr4:174217026..174252627hg19UCSC Ensembl
Outerchr4:174453601..174489202hg18UCSC Ensembl
Outerchr4:174591756..174627357hg17UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3835602
hg1935602
hg1835602
hg1735602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8032, nssv4676
SamplesNA12156, NA19129
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)nsv4610
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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