A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831072



Internal ID6156796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100162503..100362835hg19UCSC Ensembl
Outerchr7:100000439..100200771hg18UCSC Ensembl
Outerchr7:99807154..100007486hg17UCSC Ensembl
Cytoband7q22.1
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 Variantsnssv1446310, nssv1446308, nssv1446300, nssv1446303, nssv1446304, nssv1446305, nssv1446302, nssv1446306, nssv1446301, nssv1446299, nssv1446309
Samples
Known GenesACTL6B, AGFG2, EPO, FBXO24, GIGYF1, GNB2, LOC100129845, LRCH4, MOSPD3, PCOLCE, POP7, SAP25, TFR2, ZAN
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831072
Frequency
Sample Size95
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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