A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015764



Internal ID19104982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65190920..65719808hg38UCSC Ensembl
Innerchr7:64651298..65184781hg19UCSC Ensembl
Innerchr7:64288733..64822216hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38528889
hg19533484
hg18533484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6435n100
Supporting Variantsnssv3655566
Samples
Known GenesINTS4L2, LOC441242, ZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015764
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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