A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832324



Internal ID6158048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:6889463..7041469hg19UCSC Ensembl
Outerchr12:6759724..6911730hg18UCSC Ensembl
Outerchr12:6759724..6911730hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1449586, nssv1449585
Samples
Known GenesATN1, CD4, CDCA3, DSTNP2, ENO2, GNB3, GPR162, LEPREL2, LRRC23, RPL13P5, SPSB2, TPI1, USP5
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832324
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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