A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607749



Internal ID16048472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89218730..89261877hg38UCSC Ensembl
Innerchr7:88848044..88891191hg19UCSC Ensembl
Innerchr7:88685980..88729127hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3843148
hg1943148
hg1843148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155358
SamplesNINDS_2
Known GenesZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607749
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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