A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515777



Internal ID15096384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146528356..146557568hg38UCSC Ensembl
Innerchr7:146225448..146254660hg19UCSC Ensembl
Innerchr7:145856381..145885593hg18UCSC Ensembl
Innerchr7:145663096..145692308hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3829213
hg1929213
hg1829213
hg1729213
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691783, nssv675650, nssv680401, nssv681860, nssv660855, nssv669873, nssv659316, nssv678409, nssv678740, nssv693117, nssv690052, nssv683717, nssv690718, nssv664746, nssv668863
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515777
Frequency
Sample Size2026
Observed Gain5
Observed Loss10
Observed Complex0
Frequencyn/a


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