A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029556



Internal ID19118775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136849940hg38UCSC Ensembl
Innerchr8:137681619..137862183hg19UCSC Ensembl
Innerchr8:137750801..137931365hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38180565
hg19180565
hg18180565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3757396, nssv3692770, nssv3692766, nssv3692767, nssv3692783, nssv3757394, nssv3692769, nssv3757399, nssv3757397, nssv3757395, nssv3692777, nssv3692759, nssv3692764, nssv3692776, nssv3692781, nssv3692760, nssv3692780, nssv3692774, nssv3692757, nssv3692771, nssv3692763, nssv3757393, nssv3692761, nssv3692782, nssv3692779, nssv3692762, nssv3692778, nssv3692756, nssv3692775, nssv3757398, nssv3692768, nssv3692765, nssv3692772, nssv3692758, nssv3757400, nssv3692773
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029556
Frequency
Sample Size11257
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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